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FDA 510(k)

SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT

K-Number: K850274 · 1985-04-25

ApplicantSutter Biomedical, Inc.
Decision Date1985-04-25
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT is the device name listed in this FDA 510(k) record. The listed applicant is Sutter Biomedical, Inc.. It received FDA 510(k) clearance on 1985-04-25 under 510(k) number K850274. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT?

SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT is a medical device that received FDA 510(k) clearance on 1985-04-25. The listed applicant is Sutter Biomedical, Inc.. The 510(k) number is K850274.

When did SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT receive FDA 510(k) clearance?

SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT received FDA 510(k) clearance on 1985-04-25, under 510(k) number K850274.

Who is the listed applicant for SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT?

The FDA 510(k) record lists Sutter Biomedical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT?

The FDA product code for SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT is BXB.

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Other records listing Sutter Biomedical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K875249SUTTER PHALANGEAL CAPK870200SUTTER FINGER JOINT PROSTHESISK861983SUTTER LESSER METATARSAL CAPK830974SUTTER CPM 5000K830649SUTTER CPM 2000K823539SUTTER CPM

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Related Devices (Code: BXB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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