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

SAFE T COUNT

K Number: K802865 · Decision Dec 18, 1980
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
66
Applicant Total
10
Review Days
36

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Basic Information

Device Name
SAFE T COUNT
K Number
K802865
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 12, 1980
Decision Date
December 18, 1980
Product Code
KDC
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
KDC Instrument, Surgical, Disposable

Similar 510(k) Clearances

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

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Other Clearances by Instranetics, Inc.

K Number Device Name
K823430 INSTRA-SAFE
K811824 CAUTERY CADDY PAD
K811823 SHARPS CADDY FB
K811822 TIP-VU
K810294 LINE CADDY
K810208 BLADE SAFE
K802866 SHARPS CADDY MAGNETIC & SHARPS CADDY FOA
K781575 DISPOSABLE LYMPHANGIOGRAM SET
K770894 NEURO-SORB PATTIES