ANESTHESIA/RETROBULBAR NEEDLES— 510(k) K880347

Substantially Equivalent

Myocure, Inc.

FDA 510(k) clearance K880347 for ANESTHESIA/RETROBULBAR NEEDLES, Substantially Equivalent on 1988-05-03. Applicant: Myocure, Inc..

Clearance details

Applicant: Myocure, Inc.
Product code: Code HMX
Advisory panel: Ophthalmic
Date received: 1988-01-26
Decision date: 1988-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glendale, CA, US

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Adverse events under product code HMX

product code HMX

Other: 1
Total: 1

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.