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FDA 510(k)

MOBILIMB HAND C.P.M. UNIT

K-Number: K880336 · 1988-02-16

ApplicantToronto Medical Corp.
Decision Date1988-02-16
Product CodeJFA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOBILIMB HAND C.P.M. 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 1988-02-16 under 510(k) number K880336. The device is classified under product code JFA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOBILIMB HAND C.P.M. UNIT?

MOBILIMB HAND C.P.M. UNIT is a medical device that received FDA 510(k) clearance on 1988-02-16. The listed applicant is Toronto Medical Corp.. The 510(k) number is K880336.

When did MOBILIMB HAND C.P.M. UNIT receive FDA 510(k) clearance?

MOBILIMB HAND C.P.M. UNIT received FDA 510(k) clearance on 1988-02-16, under 510(k) number K880336.

Who is the listed applicant for MOBILIMB HAND C.P.M. 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 HAND C.P.M. UNIT?

The FDA product code for MOBILIMB HAND C.P.M. UNIT is JFA.

Related Clinical Trials

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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 UNITK900466MOBILIMB W1 WRIST CPM UNITK900795MOBILIMB L4 LOWER LIMB CPM UNIT

View all 11 devices →

Related Devices (Code: JFA)

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.

K945803THERMAFLEX, MODEL SD 55 C.P.M.H.Burke Neutech, Inc.K931016JACE MODEL H440 HAND CPM DEVICEJace Systems, Inc.K933418HAND THERAPY ASSOSTBardon Ent., Inc.K921351JACE MODEL PM-410 HAND CPM DEVICEJace Systems, Inc.K900794MOBILIMB H3 HAND CPM UNITToronto Medical Corp.K900581DANNIFLEX CPM 880(TM)Buckman Co., Inc.

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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