FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AUTOCLIX

K Number: K810075 · Decision Feb 4, 1981
Classifications
1
FEI Numbers
157
Registration Numbers
157
Same Product Code
109
Applicant Total
21
Review Days
22

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Basic Information

Device Name
AUTOCLIX
K Number
K810075
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4850
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Biodynamics Corp.
Date Received
January 13, 1981
Decision Date
February 4, 1981
Product Code
FMK
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
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Similar 510(k) Clearances

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

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Other Clearances by Biodynamics Corp.

K Number Device Name
K051675 BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER
K884033 BIODYNAMICS MODEL 200 BODY COMPOSITION ANALYZER
K881631 BIODYNAMICS AUTOTRANSFUSION RESERVOIR
K881968 BIODYNAMICS MODEL BI-400 BODY COMPOSITION ANALYZER
K874361 BIODYNAMICS MODEL BI-300 BODY COMPOSITION ANALYZER
K873807 AUTOTRANSFUSION APPARATUS
K874034 ADR-22 AUTOMATIC DIALYZER REPROCESSOR
K870052 INFUMIX MIXING CONTAINER
K822716 UNIVERSAL CENTRIFUGE
K822715 PLATELET CENTRIFUGE
Search all 21 clearances from Biodynamics Corp. →