FDA Browser
by
Innolitics
Anesthesiology
Review Panel
Cardiovascular
Review Panel
Chemistry
Review Panel
Dental
Review Panel
Ear, Nose, Throat
Review Panel
Gastroenterology and Urology
Review Panel
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
Miscellaneous
Miscellaneous
Subpart B—Diagnostic Devices
CFR Sub-Part
GCI
Laryngoscope, Endoscope
2
Product Code
K
02
1747
DEGALL LAPAROSCOPIC GALLBLADDER EXTRACTOR
2
Cleared 510(K)
K
00
3222
MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTER
2
Cleared 510(K)
K
00
1362
KARL STORZ 3D VIDEO SYSTEM
2
Cleared 510(K)
K
93
3515
BOOTY ENDOSCOPE WARMER
2
Cleared 510(K)
K
93
0302
BIRTCHER SURE CLEAN INSTRUMENT SYSTEM
2
Cleared 510(K)
K
93
0496
GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPS
2
Cleared 510(K)
K
92
2123
AUTO SUTURE DISPOSABLE ENDOSCOPIC SPECIMEN POUCH
2
Cleared 510(K)
K
92
0139
GLEESON CLOT-BUSTER
2
Cleared 510(K)
K
91
5762
POOLE TIP SUCTION PROBE
2
Cleared 510(K)
K
91
4120
SINGLE USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT
2
Cleared 510(K)
Show All 14 Submissions
GCJ
Laparoscope, General & Plastic Surgery
2
Product Code
MFJ
Device, Endoscopic Suturing
2
Product Code
EPY
Speculum, Ent
1
Product Code
NAY
System, Surgical, Computer Controlled Instrument
2
Product Code
NEQ
Device, Telemedicine, Robotic
2
Product Code
PDT
Burn Resuscitation Decision Support Software
2
Product Code
FDP
Apparatus, Pneumoperitoneum, Automatic
2
Product Code
GCG
Peritoneoscope
2
Product Code
GCH
Mediastinoscope, Diagnostic
2
Product Code
OTJ
Laparoscopic Single Port Access Device
2
Product Code
OWN
Confocal Optical Imaging
2
Product Code
QGY
Mobile / Tablet Software Application To Control Settings Of Surgical And Endoscopic Camera
2
Product Code
NQQ
System, Imaging, Optical Coherence Tomography (Oct)
2
Product Code
POY
Post Breast Biopsy Hemostatic Breast Compression Device
2
Product Code
FXE
Speculum, Non-Illuminated
1
Product Code
FXF
Speculum, Illuminated
1
Product Code
FXG
Specula Accessories
1
Product Code
JYK
Holder, Ear Speculum
1
Product Code
KAG
Holder, Speculum, Ent
1
Product Code
QSM
System, Surgical, Computer Controlled Instrument, Remanufactured
2
Product Code
QZB
Software Controlled Endoscope And Instrument Holder
2
Product Code
Subpart C—General Hospital and Personal Use Monitoring Devices
CFR Sub-Part
Subpart D—Prosthetic Devices
CFR Sub-Part
Subpart E—Neurological Surgical Devices
CFR Sub-Part
Subpart E—Surgical Devices
CFR Sub-Part
Subpart F—General Hospital and Personal Use Therapeutic Devices
CFR Sub-Part
Subpart F—Physical Medicine Therapeutic Devices
CFR Sub-Part
Subpart F—Therapeutic Devices
CFR Sub-Part
Toxicology
Review Panel
Medical Genetics
Review Panel
Unknown
Review Panel
Last synced on 16 August 2024 at 11:05 pm
SU
/
subpart-b—diagnostic-devices
/
GCI
/
K930302
View Source
BIRTCHER SURE CLEAN INSTRUMENT SYSTEM
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930302
510(k) Type
Traditional
Applicant
BIRTCHER MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/1993
Days to Decision
279 days
Submission Type
Statement
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Neurology
Obstetrical and Gynecological
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Miscellaneous
Subpart B—Diagnostic Devices
GCI
Laryngoscope, Endoscope
K
02
1747
DEGALL LAPAROSCOPIC GALLBLADDER EXTRACTOR
K
00
3222
MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTER
K
00
1362
KARL STORZ 3D VIDEO SYSTEM
K
93
3515
BOOTY ENDOSCOPE WARMER
K
93
0302
BIRTCHER SURE CLEAN INSTRUMENT SYSTEM
K
93
0496
GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPS
K
92
2123
AUTO SUTURE DISPOSABLE ENDOSCOPIC SPECIMEN POUCH
K
92
0139
GLEESON CLOT-BUSTER
K
91
5762
POOLE TIP SUCTION PROBE
K
91
4120
SINGLE USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT
Show All 14 Submissions
GCJ
Laparoscope, General & Plastic Surgery
MFJ
Device, Endoscopic Suturing
EPY
Speculum, Ent
NAY
System, Surgical, Computer Controlled Instrument
NEQ
Device, Telemedicine, Robotic
PDT
Burn Resuscitation Decision Support Software
FDP
Apparatus, Pneumoperitoneum, Automatic
GCG
Peritoneoscope
GCH
Mediastinoscope, Diagnostic
OTJ
Laparoscopic Single Port Access Device
OWN
Confocal Optical Imaging
QGY
Mobile / Tablet Software Application To Control Settings Of Surgical And Endoscopic Camera
NQQ
System, Imaging, Optical Coherence Tomography (Oct)
POY
Post Breast Biopsy Hemostatic Breast Compression Device
FXE
Speculum, Non-Illuminated
FXF
Speculum, Illuminated
FXG
Specula Accessories
JYK
Holder, Ear Speculum
KAG
Holder, Speculum, Ent
QSM
System, Surgical, Computer Controlled Instrument, Remanufactured
QZB
Software Controlled Endoscope And Instrument Holder
Subpart C—General Hospital and Personal Use Monitoring Devices
Subpart D—Prosthetic Devices
Subpart E—Neurological Surgical Devices
Subpart E—Surgical Devices
Subpart F—General Hospital and Personal Use Therapeutic Devices
Subpart F—Physical Medicine Therapeutic Devices
Subpart F—Therapeutic Devices
Toxicology
Medical Genetics
Unknown
SU
/
subpart-b—diagnostic-devices
/
GCI
/
K930302
View Source
BIRTCHER SURE CLEAN INSTRUMENT SYSTEM
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930302
510(k) Type
Traditional
Applicant
BIRTCHER MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/1993
Days to Decision
279 days
Submission Type
Statement