Padac

FDA 510(k) K812458 · Calbiochem-Behring Corp.

Substantially Equivalent

510(k) numberK812458

Submission

Device name
Padac
Applicant
Calbiochem-Behring Corp.
Mchenry, IL, US
Received
August 31, 1981
Decision date
September 23, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JTO – Discs, Strips And Reagents, Microorganism Differentiation
Device class
Class I (low risk)
Regulation
21 CFR 866.2660
Specialty
Microbiology

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K820088Aft System Proficiency Testing ProgramDBL · Traditional 01/26/1982SE
K810718C-Peptice ReagentsJKD · Traditional 03/31/1981SE
K810669Pantrak E.K.CIW · Traditional 03/31/1981SE
K810404Rheumatoid Factors Reference SerumDHR · Traditional 03/11/1981SE
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Questions and answers

When was Padac cleared by the FDA?

Padac (K812458) received a 510(k) decision of Substantially Equivalent on September 23, 1981, 23 days after the submission was received.

What is the product code of K812458?

The FDA product code is JTO – Discs, Strips And Reagents, Microorganism Differentiation, a Class I (low risk) device regulated under 21 CFR 866.2660.