PFIZER/AS&E 0450 LOCALIZER— 510(k) K800501

Name: FDA 510(k) clearance K800501
Creator: U.S. Food and Drug Administration
Published: 1980-04-10

Substantially Equivalent

Pfizer Medical Systems, Inc.

FDA 510(k) clearance K800501 for PFIZER/AS&E 0450 LOCALIZER, Substantially Equivalent on 1980-04-10. Applicant: Pfizer Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Pfizer Medical Systems, Inc.
Product code: Code JDX
Device class: Class 2
Regulation: 21 CFR 888.4580
Advisory panel: Orthopedic
Date received: 1980-03-04
Decision date: 1980-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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