MYOCUR BLADE PAC— 510(k) K822392

Substantially Equivalent

Myocure, Inc.

FDA 510(k) clearance K822392 for MYOCUR BLADE PAC, Substantially Equivalent on 1982-08-25. Applicant: Myocure, Inc.. Device class: 3.

Clearance details

Applicant: Myocure, Inc.
Product code: Code HMN
Device class: Class 3
Advisory panel: Unknown
Date received: 1982-08-09
Decision date: 1982-08-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

More clearances from Myocure, Inc.

K880345 — CYSTOTOMES/KNIFES1988-05-03
K880346 — CANNULAS1988-05-03
K880347 — ANESTHESIA/RETROBULBAR NEEDLES1988-05-03
K874057 — OPHTHALMIC TIP & BLADE SCALPELS1987-12-23
K874056 — OPHTHALMIC DISPOSABLE BLADES1987-12-22

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