PROPPER SUPER SERACULT(R)— 510(k) K921798

Name: FDA 510(k) clearance K921798
Creator: U.S. Food and Drug Administration
Published: 1992-10-05

Substantially Equivalent

Propper Mfg. Co., Inc.

FDA 510(k) clearance K921798 for PROPPER SUPER SERACULT(R), Substantially Equivalent on 1992-10-05. Applicant: Propper Mfg. Co., Inc.. Device class: 2.

Clearance details

Applicant: Propper Mfg. Co., Inc.
Product code: Code KHE
Device class: Class 2
Regulation: 21 CFR 864.6550
Advisory panel: Hematology
Date received: 1992-04-14
Decision date: 1992-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Long Island City, NY, US

Download summary PDF View on FDA.gov ↗

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