SUTTER CPM— 510(k) K820083

Substantially Equivalent

Sutter Biomedical, Inc.

FDA 510(k) clearance K820083 for SUTTER CPM, Substantially Equivalent on 1982-01-28. 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: 1982-01-12
Decision date: 1982-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Sutter Biomedical, Inc.

K875249 — SUTTER PHALANGEAL CAP1988-02-03
K870200 — SUTTER FINGER JOINT PROSTHESIS1987-10-09
K861983 — SUTTER LESSER METATARSAL CAP1986-09-08
K850274 — SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT1985-04-25
K830974 — SUTTER CPM 50001983-04-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.