PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL.— 510(k) K803032

Name: FDA 510(k) clearance K803032
Creator: U.S. Food and Drug Administration
Published: 1981-01-22

Substantially Equivalent

Pfizer Medical Systems, Inc.

FDA 510(k) clearance K803032 for PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL., Substantially Equivalent on 1981-01-22. Applicant: Pfizer Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Pfizer Medical Systems, Inc.
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 1980-12-01
Decision date: 1981-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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