FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
FLEXIBLE LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER
K Number: K944790
·
Decision Nov 29, 1994
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
23
Applicant Total
58
Review Days
62
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Basic Information
- Device Name
- FLEXIBLE LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER
- K Number
- K944790
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4200
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Applied Medical Resources
- Date Received
- September 28, 1994
- Decision Date
- November 29, 1994
- Product Code
- GBZ
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| GBZ | Catheter, Cholangiography | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (GBZ), ordered by most recent decision date.
PRE-VIEW CHOLANGIOGRAPHY CLAMP
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ENDOPATH
FDA 510(k)
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MICROVASIVE INSURG CHLOANGIOGRAPHIC CATHETER
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TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE
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STRYKER ENDOSCOPY CHOLANGIOGRAM KIT
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FDA Class 1
·General, Plastic Surgery
ANGIOLAPCATH CHOLANGIOGRAPHY KIT
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
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