FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CATHETER, CHOLANGIOGRAM, OPERATIVE

K Number: K772288 · Decision Jan 30, 1978
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
23
Applicant Total
26
Review Days
49

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Basic Information

Device Name
CATHETER, CHOLANGIOGRAM, OPERATIVE
K Number
K772288
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Gesco Intl., Inc.
Date Received
December 12, 1977
Decision Date
January 30, 1978
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
GBZ Catheter, Cholangiography

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GBZ), ordered by most recent decision date.

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Other Clearances by Gesco Intl., Inc.

K Number Device Name
K954422 PER-Q-CATH MID-LINE
K940953 UMBILI-CATH-S
K940870 UMBILI-CATH
K940952 UMBILI-CATH-S-DL
K941672 URI-CATH CATHETER
K941232 THORA-CATH
K940871 UMBILI-CATH-P
K931989 VENTRI-CATH
K926063 PER-Q-CATH DRESSING CHANGE TRAY
K923591 PALA-NATE
Search all 26 clearances from Gesco Intl., Inc. →