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FDA 510(k)

MOBILIMB W1 WRIST CPM UNIT

K-Number: K900466 · 1990-03-12

ApplicantToronto Medical Corp.
Decision Date1990-03-12
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOBILIMB W1 WRIST CPM UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Toronto Medical Corp.. It received FDA 510(k) clearance on 1990-03-12 under 510(k) number K900466. 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 MOBILIMB W1 WRIST CPM UNIT?

MOBILIMB W1 WRIST CPM UNIT is a medical device that received FDA 510(k) clearance on 1990-03-12. The listed applicant is Toronto Medical Corp.. The 510(k) number is K900466.

When did MOBILIMB W1 WRIST CPM UNIT receive FDA 510(k) clearance?

MOBILIMB W1 WRIST CPM UNIT received FDA 510(k) clearance on 1990-03-12, under 510(k) number K900466.

Who is the listed applicant for MOBILIMB W1 WRIST CPM UNIT?

The FDA 510(k) record lists Toronto Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOBILIMB W1 WRIST CPM UNIT?

The FDA product code for MOBILIMB W1 WRIST CPM UNIT is BXB.

Related Clinical Trials

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.

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Other records listing Toronto Medical Corp. 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.

K950682W2 WRIST CPM UNITK935587MULTILINK SHOULDER CPM UNITK935841DR KOOLK925926MOBILIMB T1 TOE CPM UNITK900795MOBILIMB L4 LOWER LIMB CPM UNITK900794MOBILIMB H3 HAND CPM UNIT

View all 11 devices →

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.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.K955106BTE CPM-20Baltimore 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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