REACTIFS, IBF ULTROGELS ACA & ULTROGELS A— 510(k) K844164

Substantially Equivalent

Lkb Instruments, Inc.

FDA 510(k) clearance K844164 for REACTIFS, IBF ULTROGELS ACA & ULTROGELS A, Substantially Equivalent on 1984-12-10. Applicant: Lkb Instruments, Inc..

Clearance details

Applicant: Lkb Instruments, Inc.
Product code: Code DII
Advisory panel: Clinical Chemistry
Date received: 1984-10-25
Decision date: 1984-12-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gaithersburg, MD, US

Download summary PDF View on FDA.gov ↗

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