SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT— 510(k) K850274

Name: FDA 510(k) clearance K850274
Creator: U.S. Food and Drug Administration
Published: 1985-04-25

Substantially Equivalent

Sutter Biomedical, Inc.

FDA 510(k) clearance K850274 for SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT, Substantially Equivalent on 1985-04-25. Applicant: Sutter Biomedical, Inc.. Device class: 1.

Clearance details

Applicant: Sutter Biomedical, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1985-01-23
Decision date: 1985-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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