Cleared Traditional

PHADEBAS RAST(R)/PHADEZYM(R) RAST ALLERGEN DISC

K893132 · Pharmacia, Inc. · Immunology
Jun 1989
Decision
38d
Days
Class 2
Risk

About This 510(k) Submission

K893132 is an FDA 510(k) clearance for the PHADEBAS RAST(R)/PHADEZYM(R) RAST ALLERGEN DISC, a System, Test, Radioallergosorbent (rast) Immunological (Class II — Special Controls, product code DHB), submitted by Pharmacia, Inc. (Piscataway, US). The FDA issued a Cleared decision on June 2, 1989, 38 days after receiving the submission on April 25, 1989. This device falls under the Immunology review panel. Regulated under 21 CFR 866.5750.

Submission Details

510(k) Number K893132 FDA.gov
FDA Decision Cleared SESE
Date Received April 25, 1989
Decision Date June 02, 1989
Days to Decision 38 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary

Device Classification

Product Code DHB — System, Test, Radioallergosorbent (rast) Immunological
Device Class Class II — Special Controls
CFR Regulation 21 CFR 866.5750

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