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FDA 510(k)

MONITORING SYSTEM, REHABILITATION

K-Number: K760510 · 1976-08-30

Decision Date1976-08-30
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MONITORING SYSTEM, REHABILITATION is the device name listed in this FDA 510(k) record. The listed applicant is Medcraft Corp.. It received FDA 510(k) clearance on 1976-08-30 under 510(k) number K760510. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONITORING SYSTEM, REHABILITATION?

MONITORING SYSTEM, REHABILITATION is a medical device that received FDA 510(k) clearance on 1976-08-30. The listed applicant is Medcraft Corp.. The 510(k) number is K760510.

When did MONITORING SYSTEM, REHABILITATION receive FDA 510(k) clearance?

MONITORING SYSTEM, REHABILITATION received FDA 510(k) clearance on 1976-08-30, under 510(k) number K760510.

Who is the listed applicant for MONITORING SYSTEM, REHABILITATION?

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

What is the FDA product code for MONITORING SYSTEM, REHABILITATION?

The FDA product code for MONITORING SYSTEM, REHABILITATION is DPS.

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 Medcraft 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.

Related Devices (Code: DPS)

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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