FLEISCHMAN-SWARTZ ENDO-OCULAR PROBE (STERILE)— 510(k) K860358

Substantially Equivalent

Hgm, Inc.

FDA 510(k) clearance K860358 for FLEISCHMAN-SWARTZ ENDO-OCULAR PROBE (STERILE), Substantially Equivalent on 1986-03-21. Applicant: Hgm, Inc..

Clearance details

Applicant: Hgm, Inc.
Product code: Code HQF
Advisory panel: Ophthalmic
Date received: 1986-01-30
Decision date: 1986-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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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.