RUBELLA RQ BIO-ENZABEAD KIT— 510(k) K821804

Substantially Equivalent

Litton Bionetics

FDA 510(k) clearance K821804 for RUBELLA RQ BIO-ENZABEAD KIT, Substantially Equivalent on 1982-09-14. Applicant: Litton Bionetics. Device class: 2.

Clearance details

Applicant: Litton Bionetics
Product code: Code LFX
Device class: Class 2
Regulation: 21 CFR 866.3510
Advisory panel: Microbiology
Date received: 1982-06-17
Decision date: 1982-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Litton Bionetics

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K831343 — CMV RQ BIO-ENZABEAD KIT1983-08-08
K822985 — EBV-M KIT1982-12-03
K801720 — TOXO BIO-BEAD TITRATION KIT1980-09-16

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