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

ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER

K Number: K871424 · Decision Jul 8, 1987
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
1
Applicant Total
23
Review Days
90

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Basic Information

Device Name
ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER
K Number
K871424
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4490
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Hgm, Inc.
Date Received
April 9, 1987
Decision Date
July 8, 1987
Product Code
LMS
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
LMS Laser, Microsurgical Argon, For Uses Other Than Otology, Including Laryngology & General Use In Otolaryngology

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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
K873773 ENDOCOAGULATOR MODELS 8 AND 20 ARGON LASER
K872630 ENDOCOAGULATOR(TM) MODEL 20 ARGON LASER FOR UROLO.
Search all 23 clearances from Hgm, Inc. →