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

ELECTROSURGICAL UNIT

K Number: K981781 · Decision Dec 4, 1998
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
10
Review Days
198

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Basic Information

Device Name
ELECTROSURGICAL UNIT
K Number
K981781
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hill-Med, Inc.
Date Received
May 20, 1998
Decision Date
December 4, 1998
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

Similar 510(k) Clearances

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

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Other Clearances by Hill-Med, Inc.

K Number Device Name
K993991 HM-930 ELECTROSURGICAL UNIT
K961473 HM-88011 SOLID STATE ELECTR SURGICAL UNIT
K951718 HM-SPIRO
K940140 HM-CRYO
K932782 HM-0660
K932896 HM-0690 COLPOSCOPE
K932817 HM-880 I
K932818 HM-880
K932720 HM-0970