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

INSTRA-SAFE

K Number: K823430 · Decision Jan 7, 1983
Classifications
1
FEI Numbers
875
Registration Numbers
875
Same Product Code
75
Applicant Total
10
Review Days
52

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Basic Information

Device Name
INSTRA-SAFE
K Number
K823430
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Instranetics, Inc.
Date Received
November 16, 1982
Decision Date
January 7, 1983
Product Code
FSM
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
FSM Tray, Surgical, Instrument

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Other Clearances by Instranetics, Inc.

K Number Device Name
K811824 CAUTERY CADDY PAD
K811823 SHARPS CADDY FB
K811822 TIP-VU
K810294 LINE CADDY
K810208 BLADE SAFE
K802865 SAFE T COUNT
K802866 SHARPS CADDY MAGNETIC & SHARPS CADDY FOA
K781575 DISPOSABLE LYMPHANGIOGRAM SET
K770894 NEURO-SORB PATTIES