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Innolitics
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Review Panel
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Miscellaneous
Miscellaneous
NRZ
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
3
Product Code
OVX
Water Immersion Labor Pool
N
Product Code
PAS
Rf/Microwave Hyperthermia System, Cancer Treatment
F
Product Code
HHY
Prosthesis, Suture, Cerclage
3
Product Code
LHD
Device, Fertility Diagnostic, Proceptive
U
Product Code
LLQ
Cap, Cervical, Contraceptive
3
Product Code
LLX
Catheter, Sampling, Chorionic Villus
3
Product Code
LOB
Dilator, Cervical, Synthetic, Osmotic, Pregnancy Termination
3
Product Code
LTA
Fluid, Hysteroscopy
3
Product Code
LTY
Fluid, Cytological Collection
3
Product Code
MCI
Graft, Vascular, Hemodialysis Access, Synthetic/Biological Composite
3
Product Code
MCN
Barrier, Absorbable, Adhesion
3
Product Code
MCP
Stimulator, Fetal, Acoustic
3
Product Code
MGI
Aspirator, Ultrasonic
3
Product Code
MKN
Catheter, Balloon, Transcervical
3
Product Code
MMA
Oximeter, Fetal Pulse
3
Product Code
MNB
Device, Thermal Ablation, Endometrial
3
Product Code
MPR
Stent, Bladder, Fetal
F
Product Code
MPT
Contraception Calculator
U
Product Code
K
95
4183
OVULATION CALCULATOR/CONCEPTION CALCULATOR
U
Cleared 510(K)
K
82
1836
PREGNANCY (W) EDGE
U
Cleared 510(K)
K
81
0832
FORECASTER
U
Cleared 510(K)
MWM
Sensor, Electro-Optical (For Cervical Cancer)
3
Product Code
PKF
D And C Tray
N
Product Code
QLH
System, Intravaginal, For Controlled Release Of Drug Substance, Cder Or Cber Led
N
Product Code
QRZ
External Condom For Anal Intercourse Or Vaginal Intercourse
2
Product Code
Submissions with No Product Code
Miscellaneous
Subpart B—Clinical Chemistry Test Systems
CFR Sub-Part
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—Obstetrical and Gynecological Monitoring Devices
CFR Sub-Part
Subpart D—Cardiovascular Prosthetic Devices
CFR Sub-Part
Subpart D—Obstetrical and Gynecological Prosthetic Devices
CFR Sub-Part
Subpart D—Physical Medicine Prosthetic Devices
CFR Sub-Part
Subpart D—Prosthetic Devices
CFR Sub-Part
Subpart E—Obstetrical and Gynecological Surgical Devices
CFR Sub-Part
Subpart F—Obstetrical and Gynecological Therapeutic Devices
CFR Sub-Part
Subpart F—Therapeutic Devices
CFR Sub-Part
Subpart G—Assisted Reproduction Devices
CFR Sub-Part
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 20 December 2024 at 11:05 pm
OB
/
OB-misc
/
MPT
/
K821836
View Source
PREGNANCY (W) EDGE
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K821836
510(k) Type
Traditional
Applicant
BODY THERAPEUTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1982
Days to Decision
38 days
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Neurology
Obstetrical and Gynecological
Miscellaneous
NRZ
Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided
OVX
Water Immersion Labor Pool
PAS
Rf/Microwave Hyperthermia System, Cancer Treatment
HHY
Prosthesis, Suture, Cerclage
LHD
Device, Fertility Diagnostic, Proceptive
LLQ
Cap, Cervical, Contraceptive
LLX
Catheter, Sampling, Chorionic Villus
LOB
Dilator, Cervical, Synthetic, Osmotic, Pregnancy Termination
LTA
Fluid, Hysteroscopy
LTY
Fluid, Cytological Collection
MCI
Graft, Vascular, Hemodialysis Access, Synthetic/Biological Composite
MCN
Barrier, Absorbable, Adhesion
MCP
Stimulator, Fetal, Acoustic
MGI
Aspirator, Ultrasonic
MKN
Catheter, Balloon, Transcervical
MMA
Oximeter, Fetal Pulse
MNB
Device, Thermal Ablation, Endometrial
MPR
Stent, Bladder, Fetal
MPT
Contraception Calculator
K
95
4183
OVULATION CALCULATOR/CONCEPTION CALCULATOR
K
82
1836
PREGNANCY (W) EDGE
K
81
0832
FORECASTER
MWM
Sensor, Electro-Optical (For Cervical Cancer)
PKF
D And C Tray
QLH
System, Intravaginal, For Controlled Release Of Drug Substance, Cder Or Cber Led
QRZ
External Condom For Anal Intercourse Or Vaginal Intercourse
Submissions with No Product Code
Subpart B—Clinical Chemistry Test Systems
Subpart B—Diagnostic Devices
Subpart B—Obstetrical and Gynecological Diagnostic Devices
Subpart C—Cardiovascular Monitoring Devices
Subpart C—Obstetrical and Gynecological Monitoring Devices
Subpart D—Cardiovascular Prosthetic Devices
Subpart D—Obstetrical and Gynecological Prosthetic Devices
Subpart D—Physical Medicine Prosthetic Devices
Subpart D—Prosthetic Devices
Subpart E—Obstetrical and Gynecological Surgical Devices
Subpart F—Obstetrical and Gynecological Therapeutic Devices
Subpart F—Therapeutic Devices
Subpart G—Assisted Reproduction Devices
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
OB
/
OB-misc
/
MPT
/
K821836
View Source
PREGNANCY (W) EDGE
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K821836
510(k) Type
Traditional
Applicant
BODY THERAPEUTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1982
Days to Decision
38 days