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

ENDOCOAGULATOR MODELS 8 AND 20 ARGON LASER

K Number: K873773 · Decision Oct 13, 1987
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
23
Review Days
27

Basic Information

Device Name
ENDOCOAGULATOR MODELS 8 AND 20 ARGON LASER
K Number
K873773
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
HGM, INC.
Date Received
September 16, 1987
Decision Date
October 13, 1987
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

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Other Clearances by HGM, INC.

K Number Device Name
K950120 SMART PLUG
K931072 HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE
K931784 HGM ILLUMINATING IMAGING ENDOCULAR PROBE
K933333 HGM SCANMAN PLUS
K931499 Q-11 OPHTHALMIC LASER
K925663 HGM ASPIRATING ENDOOCULAR(TM) PROBE
K930543 E-25 KRYPTON ION LASER (SURGICA K5)
K880908 MODEL PC ARGON LASER
K872630 ENDOCOAGULATOR(TM) MODEL 20 ARGON LASER FOR UROLO.
K870773 ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER
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