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

PADLESS ELECTROSURGICAL PENCIL

K Number: K952792 · Decision Aug 28, 1995
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
12
Review Days
70

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Basic Information

Device Name
PADLESS ELECTROSURGICAL PENCIL
K Number
K952792
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
Lca, Inc.
Date Received
June 19, 1995
Decision Date
August 28, 1995
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

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Other Clearances by Lca, Inc.

K Number Device Name
K944091 THE HOOK-CURVED CLOSED END/ELECT FIBER LASER DELIV SYS
K935439 SNJ SMOKE EVACUATION SUCTION WAND
K935258 HYBRID SURGICAL DEVICE MODIFICATION
K925726 ALLOY SCALPEL HANDPIECES, MODIFICATION
K931070 CLOSED END FIBEROPTIC LASER DELIVERY SYSTEM
K924160 HYBRID SURGICAL DEVICE
K923991 ZOE LASER, CONTACT ND:YAG LASER SYSTEM
K924120 MOLDED FIBER CAP DELIVERY SYSTEM
K901365 LASER FORCEPS HANDPIECE
K902562 REVISED LABELING FOR MODEL CL-0PE ND:YAG LASER
Search all 12 clearances from Lca, Inc. →