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Innolitics
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Review Panel
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Miscellaneous
Subpart B—Diagnostic Devices
CFR Sub-Part
Subpart B—Obstetrical and Gynecological Diagnostic Devices
CFR Sub-Part
Subpart C—Cardiovascular Monitoring Devices
CFR Sub-Part
Subpart C—Monitoring Devices
CFR Sub-Part
KPN
Alarm, Conditioned Response Enuresis
2
Product Code
K
13
0951
SIM
2
Cleared 510(K)
K
97
1442
HUGHES BLADDER AND BOWEL TRAINING SYSTEM(AD-T-18, MED-18,MED-1,MED-T-1,MEDD-18,MED-38,MED-T-10,MED-T-25,MED-T-5
2
Cleared 510(K)
K
97
1855
POTTY PAL AND FOREVER-DRY
2
Cleared 510(K)
K
96
2770
UROSURGE ACUTRAINER
2
Cleared 510(K)
K
96
2416
DRYTIME FOR BLADDER CONTROL SILENT
2
Cleared 510(K)
K
95
5338
DRYTIME FOR POTTY TRAINING
2
Cleared 510(K)
K
94
3559
REMOTE A'LERT
2
Cleared 510(K)
K
94
3558
PRO'TECT
2
Cleared 510(K)
K
94
2057
FISHER-PRICE DRY NIGHT MONITOR
2
Cleared 510(K)
K
93
5915
WET SENSE
2
Cleared 510(K)
K
93
4369
DRI SLEEPER
2
Cleared 510(K)
K
93
0005
DRITRAINER
2
Cleared 510(K)
K
92
1431
POTTY PAGER
2
Cleared 510(K)
K
91
1279
DRY TIME
2
Cleared 510(K)
K
90
3856
WET-NO-MORE MONITOR
2
Cleared 510(K)
K
90
1907
PROFESSIONAL MONITOR
2
Cleared 510(K)
K
90
1906
WET-NO-MORE MONITOR
2
Cleared 510(K)
K
89
5852
BUZZY BEAR ENURESIS ALARM
2
Cleared 510(K)
K
89
5251
BARD INTRAVAGINAL STIM. KIT W/(IVES(TM))
2
Cleared 510(K)
K
89
5346
DR. DRY
2
Cleared 510(K)
K
88
5345
HEALTHSHIELD
2
Cleared 510(K)
K
88
2555
ANOTRON(R) INCONTINENCE CONTROL SYSTEM
2
Cleared 510(K)
K
87
2522
BED ALERT
2
Cleared 510(K)
K
87
1787
ENURESIS ALARM
2
Cleared 510(K)
K
86
4448
THE BIOSONICS CONTINENCE CONTROL SYSTEM CCS(TM)
2
Cleared 510(K)
K
86
2683
BIOSOICS SPHINCTER TRAINING SYSTEM
2
Cleared 510(K)
K
86
2757
STARCHILD SLEEPDRY
2
Cleared 510(K)
K
85
4539
UROSTAT
2
Cleared 510(K)
K
85
0538
BED SENTRY, MODEL 50U
2
Cleared 510(K)
K
84
4866
NYTONE ENURETIC ALARM BEDWETTING DEVICE
2
Cleared 510(K)
K
84
4636
SENTRY SIGNAL ENURESIS ALARM SYSTEM
2
Cleared 510(K)
K
84
2547
WET-STOP
2
Cleared 510(K)
K
83
4311
NIGHT TRAINER
2
Cleared 510(K)
K
82
3276
BED GUARD
2
Cleared 510(K)
K
82
1546
MONITORING DEVICE ENURESIS ALARM & ACC.
2
Cleared 510(K)
K
78
2093
DETECTOR PAD
2
Cleared 510(K)
K
78
0660
NITE TRAIN'R
2
Cleared 510(K)
OQT
Prostate Lesion, Documentation, System
2
Product Code
QEF
Pressure Ulcer Management Tool
1
Product Code
Subpart D—Prosthetic Devices
CFR Sub-Part
Subpart E—Obstetrical and Gynecological Surgical Devices
CFR Sub-Part
Subpart E—Surgical Devices
CFR Sub-Part
Subpart F—Neurological Therapeutic Devices
CFR Sub-Part
Subpart F—Physical Medicine Therapeutic Devices
CFR Sub-Part
Subpart F—Therapeutic Devices
CFR Sub-Part
Subpart G—General Hospital and Personal Use Miscellaneous Devices
CFR Sub-Part
General Hospital
Review Panel
Hematology
Review Panel
Immunology
Review Panel
Microbiology
Review Panel
Neurology
Review Panel
Obstetrical and Gynecological
Review Panel
Ophthalmic
Review Panel
Orthopedic
Review Panel
Pathology
Review Panel
Physical Medicine
Review Panel
Radiology
Review Panel
General and Plastic Surgery
Review Panel
Toxicology
Review Panel
Medical Genetics
Review Panel
Unknown
Review Panel
Last synced on 16 May 2025 at 11:05 pm
GU
/
subpart-c—monitoring-devices
/
KPN
/
K872522
View Source
BED ALERT
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872522
510(k) Type
Traditional
Applicant
NITE TRAIN-R ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1988
Days to Decision
208 days
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
Miscellaneous
Subpart B—Diagnostic Devices
Subpart B—Obstetrical and Gynecological Diagnostic Devices
Subpart C—Cardiovascular Monitoring Devices
Subpart C—Monitoring Devices
KPN
Alarm, Conditioned Response Enuresis
K
13
0951
SIM
K
97
1442
HUGHES BLADDER AND BOWEL TRAINING SYSTEM(AD-T-18, MED-18,MED-1,MED-T-1,MEDD-18,MED-38,MED-T-10,MED-T-25,MED-T-5
K
97
1855
POTTY PAL AND FOREVER-DRY
K
96
2770
UROSURGE ACUTRAINER
K
96
2416
DRYTIME FOR BLADDER CONTROL SILENT
K
95
5338
DRYTIME FOR POTTY TRAINING
K
94
3559
REMOTE A'LERT
K
94
3558
PRO'TECT
K
94
2057
FISHER-PRICE DRY NIGHT MONITOR
K
93
5915
WET SENSE
K
93
4369
DRI SLEEPER
K
93
0005
DRITRAINER
K
92
1431
POTTY PAGER
K
91
1279
DRY TIME
K
90
3856
WET-NO-MORE MONITOR
K
90
1907
PROFESSIONAL MONITOR
K
90
1906
WET-NO-MORE MONITOR
K
89
5852
BUZZY BEAR ENURESIS ALARM
K
89
5251
BARD INTRAVAGINAL STIM. KIT W/(IVES(TM))
K
89
5346
DR. DRY
K
88
5345
HEALTHSHIELD
K
88
2555
ANOTRON(R) INCONTINENCE CONTROL SYSTEM
K
87
2522
BED ALERT
K
87
1787
ENURESIS ALARM
K
86
4448
THE BIOSONICS CONTINENCE CONTROL SYSTEM CCS(TM)
K
86
2683
BIOSOICS SPHINCTER TRAINING SYSTEM
K
86
2757
STARCHILD SLEEPDRY
K
85
4539
UROSTAT
K
85
0538
BED SENTRY, MODEL 50U
K
84
4866
NYTONE ENURETIC ALARM BEDWETTING DEVICE
K
84
4636
SENTRY SIGNAL ENURESIS ALARM SYSTEM
K
84
2547
WET-STOP
K
83
4311
NIGHT TRAINER
K
82
3276
BED GUARD
K
82
1546
MONITORING DEVICE ENURESIS ALARM & ACC.
K
78
2093
DETECTOR PAD
K
78
0660
NITE TRAIN'R
OQT
Prostate Lesion, Documentation, System
QEF
Pressure Ulcer Management Tool
Subpart D—Prosthetic Devices
Subpart E—Obstetrical and Gynecological Surgical Devices
Subpart E—Surgical Devices
Subpart F—Neurological Therapeutic Devices
Subpart F—Physical Medicine Therapeutic Devices
Subpart F—Therapeutic Devices
Subpart G—General Hospital and Personal Use Miscellaneous Devices
General Hospital
Hematology
Immunology
Microbiology
Neurology
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
GU
/
subpart-c—monitoring-devices
/
KPN
/
K872522
View Source
BED ALERT
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872522
510(k) Type
Traditional
Applicant
NITE TRAIN-R ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1988
Days to Decision
208 days