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

PMT FUKUSHIMA MICROSURGICAL INSTRUMENT LINE

K Number: K882793 · Decision Jul 18, 1988
Classifications
1
FEI Numbers
216
Registration Numbers
216
Same Product Code
4
Applicant Total
20
Review Days
12

Basic Information

Device Name
PMT FUKUSHIMA MICROSURGICAL INSTRUMENT LINE
K Number
K882793
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
PMT CORP.
Date Received
July 6, 1988
Decision Date
July 18, 1988
Product Code
GAF
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
GAF Spatula, Surgical, General & Plastic Surgery

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K033730 PMT SPHENOIDAL ELECTRODE AND ACCESSORY, MODEL 2101-31 AND 2102-31 SERIES
K972597 PMT NEW BEGINNINGS GELSHAPES & AMEND
K970418 PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX)
K964224 STAINLESS STEEL CORTAC CORTICAL ELECTRODE(2111)/PLANTINUM CORTAC CORTICAL ELECTRODE
K935560 PMT EXTERNAL EXTERNAL DRAINAGE SYSTEM (EDS)
K933079 ELECTROCAUTERY SYSTEM MODEL 1980
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