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FDA 510(k)

MOVIT DEVICE

K-Number: K921710 · 1992-06-29

ApplicantJohn J. Navar, M.D.
Decision Date1992-06-29
Product CodeBRY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MOVIT DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is John J. Navar, M.D.. It received FDA 510(k) clearance on 1992-06-29 under 510(k) number K921710. The device is classified under product code BRY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOVIT DEVICE?

MOVIT DEVICE is a medical device that received FDA 510(k) clearance on 1992-06-29. The listed applicant is John J. Navar, M.D.. The 510(k) number is K921710.

When did MOVIT DEVICE receive FDA 510(k) clearance?

MOVIT DEVICE received FDA 510(k) clearance on 1992-06-29, under 510(k) number K921710.

Who is the listed applicant for MOVIT DEVICE?

The FDA 510(k) record lists John J. Navar, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOVIT DEVICE?

The FDA product code for MOVIT DEVICE is BRY.

Related Clinical Trials

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Related Devices (Code: BRY)

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.

K912346MEDIKEEPERMedikeeper, Inc.K901474ANESTHESIA WORKSTATIONSiemens Life Support SystemsK871564ANESTHASSISTAnestech, Inc.K821307ANESTHECACHEMed-Life, Inc.

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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