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

TUBE, STERILE NON-CONDUCTIVE CONNECTING

K Number: K760203 · Decision Jul 19, 1976
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
7
Applicant Total
23
Review Days
11

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Basic Information

Device Name
TUBE, STERILE NON-CONDUCTIVE CONNECTING
K Number
K760203
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Ipco Corp.
Date Received
July 8, 1976
Decision Date
July 19, 1976
Product Code
GCD
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
GCD Connector, Catheter

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K842836 SAFE & SOFT MINI PADS & MAXI PADS
K842837 SAFE & SOFT MAXI SHILEDS
K842838 SAFE & SOFT PANTY SHIELDS
K841953 ULTRA SHIELD BRIEFS
K840753 AMBEZE DISPOSABLE INCONTINENCE PANTS
K840754 MAXISHIELD INCONTINENCE CARE SYSTEM
K840755 MINIGARD DISPOSABLE LINERS
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