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

HGM ASPIRATING ENDOOCULAR(TM) PROBE

K Number: K925663 · Decision Aug 17, 1993
Classifications
1
FEI Numbers
60
Registration Numbers
61
Same Product Code
179
Applicant Total
23
Review Days
280

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Basic Information

Device Name
HGM ASPIRATING ENDOOCULAR(TM) PROBE
K Number
K925663
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hgm, Inc.
Date Received
November 10, 1992
Decision Date
August 17, 1993
Product Code
HQF
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HQF Laser, Ophthalmic

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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
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.
K870773 ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER
Search all 23 clearances from Hgm, Inc. →