#50002 QUAD DIAGNOSTIC SYSTEM— 510(k) K821301

Substantially Equivalent

Biomedia, Inc.

FDA 510(k) clearance K821301 for #50002 QUAD DIAGNOSTIC SYSTEM, Substantially Equivalent on 1982-06-01. Applicant: Biomedia, Inc.. Device class: 1.

Clearance details

Applicant: Biomedia, Inc.
Product code: Code JSI
Device class: Class 1
Regulation: 21 CFR 866.2360
Advisory panel: Microbiology
Date received: 1982-05-04
Decision date: 1982-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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More clearances from Biomedia, Inc.

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K811471 — MUELLER HINTON AGAR1981-06-18
K811472 — MUELLER HINTON AGAR, POURED INTO A PLATE1981-06-18

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