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

SURGICAL DUCT CLAMP (VINE)

K Number: K882169 · Decision Jun 17, 1988
Classifications
1
FEI Numbers
270
Registration Numbers
270
Same Product Code
31
Applicant Total
44
Review Days
24

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Basic Information

Device Name
SURGICAL DUCT CLAMP (VINE)
K Number
K882169
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Henley Intl.
Date Received
May 24, 1988
Decision Date
June 17, 1988
Product Code
GDJ
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
GDJ Clamp, Surgical, General & Plastic Surgery

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Other Clearances by Henley Intl.

K Number Device Name
K943449 NEUROLOGICAL DIAGNOSTIC DEVICES
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K926287 EXERCISE BICYCLE
K926314 HYDRA FITNESS MODEL 311 TOTAL POWER
K926313 COMPUTERIZED TESTING AND EXERCISE SYSTEMS
K915864 MONOTRODE CUTANEOUS ELECTRODE
K922036 SONOPULS 591
K926316 TRUE-TRAC, STRATUS
K920983 SONOPULS 590
Search all 44 clearances from Henley Intl. →