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FDA 510(k)

CONTINUOUS ANATOMICAL PASSIVE EXERCISER

K-Number: K830122 · 1983-02-07

ApplicantZimmer, Inc.
Decision Date1983-02-07
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CONTINUOUS ANATOMICAL PASSIVE EXERCISER is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1983-02-07 under 510(k) number K830122. 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 CONTINUOUS ANATOMICAL PASSIVE EXERCISER?

CONTINUOUS ANATOMICAL PASSIVE EXERCISER is a medical device that received FDA 510(k) clearance on 1983-02-07. The listed applicant is Zimmer, Inc.. The 510(k) number is K830122.

When did CONTINUOUS ANATOMICAL PASSIVE EXERCISER receive FDA 510(k) clearance?

CONTINUOUS ANATOMICAL PASSIVE EXERCISER received FDA 510(k) clearance on 1983-02-07, under 510(k) number K830122.

Who is the listed applicant for CONTINUOUS ANATOMICAL PASSIVE EXERCISER?

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

What is the FDA product code for CONTINUOUS ANATOMICAL PASSIVE EXERCISER?

The FDA product code for CONTINUOUS ANATOMICAL PASSIVE EXERCISER 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.

Other records listing Zimmer, 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.

View all 344 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.

Official Source

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

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