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

PLUME MASTER

K Number: K913036 · Decision Sep 6, 1991
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
74
Applicant Total
9
Review Days
59

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Basic Information

Device Name
PLUME MASTER
K Number
K913036
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5070
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sorex Medical
Date Received
July 9, 1991
Decision Date
September 6, 1991
Product Code
FYD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FYD Apparatus, Exhaust, Surgical

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Other Clearances by Sorex Medical

K Number Device Name
K923843 FOGLESS
K911070 PICC-FIX
K911150 SOREX SAFE-AIR
K910315 PICC INSERTION KIT/P.I.C. & PICC EXCHANG KIT/P.E.K
K905572 EDLICH WOUND MANAGEMENT TRAY
K903740 TRACH-EZE
K902410 MEDICAL PROCEDURE TRAY
K885136 GRAFT GUARD