HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE— 510(k) K931072

Name: FDA 510(k) clearance K931072
Creator: U.S. Food and Drug Administration
Published: 1994-11-10

Substantially Equivalent

Hgm, Inc.

FDA 510(k) clearance K931072 for HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE, Substantially Equivalent on 1994-11-10. Applicant: Hgm, Inc.. Device class: 2.

Clearance details

Applicant: Hgm, Inc.
Product code: Code HJM
Device class: Class 2
Regulation: 21 CFR 886.1945
Advisory panel: Ophthalmic
Date received: 1993-03-02
Decision date: 1994-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HJM

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K972506 — INFINITECH BULLET ENDO ILLUMINATED PICK MANIPULATOR1997-10-01
K950529 — PEREGRINE DIFFUSION LIGHT PIPE1995-06-07
K945877 — WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHT1995-03-02
K933445 — DPS 100 MULTIPORT ILLUMINATION SYSTEM (MIS)1994-09-23
K940393 — PEREGRINE WIDE ANGLE LIGHT PIPE1994-09-02

More clearances from Hgm, Inc.

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K950120 — SMART PLUG1995-08-11
K931784 — HGM ILLUMINATING IMAGING ENDOCULAR PROBE1994-03-01
K933333 — HGM SCANMAN PLUS1993-09-23
K931499 — Q-11 OPHTHALMIC LASER1993-08-19
K925663 — HGM ASPIRATING ENDOOCULAR(TM) PROBE1993-08-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.