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FDA 510(k)

MOBILIMB HAND EXERCISER

K-Number: K870402 · 1987-03-16

ApplicantBiodynamic Technologies, Inc.
Decision Date1987-03-16
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOBILIMB HAND EXERCISER is the device name listed in this FDA 510(k) record. The listed applicant is Biodynamic Technologies, Inc.. It received FDA 510(k) clearance on 1987-03-16 under 510(k) number K870402. 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 HAND EXERCISER?

MOBILIMB HAND EXERCISER is a medical device that received FDA 510(k) clearance on 1987-03-16. The listed applicant is Biodynamic Technologies, Inc.. The 510(k) number is K870402.

When did MOBILIMB HAND EXERCISER receive FDA 510(k) clearance?

MOBILIMB HAND EXERCISER received FDA 510(k) clearance on 1987-03-16, under 510(k) number K870402.

Who is the listed applicant for MOBILIMB HAND EXERCISER?

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

What is the FDA product code for MOBILIMB HAND EXERCISER?

The FDA product code for MOBILIMB HAND EXERCISER is BXB.

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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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