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FDA 510(k)

HOUVA-LITE LEG UNIT #701

K-Number: K761187 · 1977-02-28

Decision Date1977-02-28
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HOUVA-LITE LEG UNIT #701 is the device name listed in this FDA 510(k) record. The listed applicant is National Biological Corp.. It received FDA 510(k) clearance on 1977-02-28 under 510(k) number K761187. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOUVA-LITE LEG UNIT #701?

HOUVA-LITE LEG UNIT #701 is a medical device that received FDA 510(k) clearance on 1977-02-28. The listed applicant is National Biological Corp.. The 510(k) number is K761187.

When did HOUVA-LITE LEG UNIT #701 receive FDA 510(k) clearance?

HOUVA-LITE LEG UNIT #701 received FDA 510(k) clearance on 1977-02-28, under 510(k) number K761187.

Who is the listed applicant for HOUVA-LITE LEG UNIT #701?

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

What is the FDA product code for HOUVA-LITE LEG UNIT #701?

The FDA product code for HOUVA-LITE LEG UNIT #701 is FTC.

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 National Biological 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.

View all 27 devices →

Related Devices (Code: FTC)

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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