TRACOR, CANNULA, BICEPTS BIPOLAR— 510(k) K790043

Substantially Equivalent

Neomed Corp.

FDA 510(k) clearance K790043 for TRACOR, CANNULA, BICEPTS BIPOLAR, Substantially Equivalent on 1979-02-08. Applicant: Neomed Corp.. Device class: 2.

Clearance details

Applicant: Neomed Corp.
Product code: Code HIN
Device class: Class 2
Regulation: 21 CFR 884.4150
Advisory panel: Obstetrics/Gynecology
Date received: 1979-01-05
Decision date: 1979-02-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Neomed Corp.

K781810 — ELECTROSURGICAL UNIT 3001-30091978-12-20
K780118 — ELECTRODE, DISPERSIVE, DISP. NEOPAD1978-02-23

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