HGM ILLUMINATING IMAGING ENDOCULAR PROBE— 510(k) K931784

Name: FDA 510(k) clearance K931784
Creator: U.S. Food and Drug Administration
Published: 1994-03-01

Substantially Equivalent

Hgm, Inc.

FDA 510(k) clearance K931784 for HGM ILLUMINATING IMAGING ENDOCULAR PROBE, Substantially Equivalent on 1994-03-01. Applicant: Hgm, Inc.. Device class: 2.

Clearance details

Applicant: Hgm, Inc.
Product code: Code HQF
Device class: Class 2
Regulation: 21 CFR 886.4390
Advisory panel: Ophthalmic
Date received: 1993-04-09
Decision date: 1994-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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More clearances from Hgm, Inc.

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K950120 — SMART PLUG1995-08-11
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K933333 — HGM SCANMAN PLUS1993-09-23
K931499 — Q-11 OPHTHALMIC LASER1993-08-19
K925663 — HGM ASPIRATING ENDOOCULAR(TM) PROBE1993-08-17

Adverse events under product code HQF

product code HQF

Injury: 166
Other: 1
Total: 167

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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