REPEX-REPEATED ENDRANGE PASSIVE EXERCISE MACHINE
K-Number: K925271 · 1993-03-31
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Device Summary
Frequently Asked Questions
What is the REPEX-REPEATED ENDRANGE PASSIVE EXERCISE MACHINE?
REPEX-REPEATED ENDRANGE PASSIVE EXERCISE MACHINE is a medical device that received FDA 510(k) clearance on 1993-03-31. The listed applicant is Repex Intl., Inc.. The 510(k) number is K925271.
When did REPEX-REPEATED ENDRANGE PASSIVE EXERCISE MACHINE receive FDA 510(k) clearance?
REPEX-REPEATED ENDRANGE PASSIVE EXERCISE MACHINE received FDA 510(k) clearance on 1993-03-31, under 510(k) number K925271.
Who is the listed applicant for REPEX-REPEATED ENDRANGE PASSIVE EXERCISE MACHINE?
The FDA 510(k) record lists Repex Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REPEX-REPEATED ENDRANGE PASSIVE EXERCISE MACHINE?
The FDA product code for REPEX-REPEATED ENDRANGE PASSIVE EXERCISE MACHINE 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.
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
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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