AMPLIFIED ELISA IGE KIT— 510(k) K862368

Substantially Equivalent

Allertec, Inc.

FDA 510(k) clearance K862368 for AMPLIFIED ELISA IGE KIT, Substantially Equivalent on 1986-07-03. Applicant: Allertec, Inc..

Clearance details

Applicant: Allertec, Inc.
Product code: Code DGC
Advisory panel: Immunology
Date received: 1986-06-24
Decision date: 1986-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Francisco, CA, US

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