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

DERMALASE

K Number: K971459 · Decision Jul 18, 1997
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
10
Review Days
88

Basic Information

Device Name
DERMALASE
K Number
K971459
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ENDO TECHNIC CORP.
Date Received
April 21, 1997
Decision Date
July 18, 1997
Product Code
GEX
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
GEX Powered Laser Surgical Instrument

Similar 510(k) Clearances

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

View all

Other Clearances by ENDO TECHNIC CORP.

K Number Device Name
K990908 MILLENNIUM
K925079 LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER)
K930756 LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECE
K925114 LAPAROSCOPIC INSTRUMENTS
K924058 TROCAR
K914825 1-125 ENDOSEED
K910200 LASER-35
K864976 SOLUSET CALCIUM DEMINERALIZING SOLUTION
K862129 SET CANAL SEALER PASTE