CENTRIA INSULIN RIA— 510(k) K791707

Substantially Equivalent

Ventrex Laboratories, Inc.

FDA 510(k) clearance K791707 for CENTRIA INSULIN RIA, Substantially Equivalent on 1979-10-17. Applicant: Ventrex Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Ventrex Laboratories, Inc.
Product code: Code CFP
Device class: Class 1
Regulation: 21 CFR 862.1405
Advisory panel: Clinical Chemistry
Date received: 1979-08-28
Decision date: 1979-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K903628 — AIA-PACK IRI1990-09-07

More clearances from Ventrex Laboratories, Inc.

K914554 — SPECIFIC IGE EIA-TURBO ASSAY1992-03-13
K913833 — VENTREX ALLERGEN DISC1992-02-21
K913434 — VENTREX COATED TUBE INTACT PTH1991-10-25
K905612 — VENTREX COATED TUBE IGE RADIOIMMUNOASSAY1991-02-21
K905636 — VENTREX COATED TUBE IGE ENZYME IMMUNOASSAY1991-02-07

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