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FDA 510(k)

HO-B-LITE VI UNIT

K-Number: K810668 · 1981-04-23

ApplicantNational Biological Corp.
Decision Date1981-04-23
Product CodeKGL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HO-B-LITE VI UNIT 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 1981-04-23 under 510(k) number K810668. The device is classified under product code KGL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HO-B-LITE VI UNIT?

HO-B-LITE VI UNIT is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is National Biological Corp.. The 510(k) number is K810668.

When did HO-B-LITE VI UNIT receive FDA 510(k) clearance?

HO-B-LITE VI UNIT received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810668.

Who is the listed applicant for HO-B-LITE VI UNIT?

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 HO-B-LITE VI UNIT?

The FDA product code for HO-B-LITE VI UNIT is KGL.

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.

K070934PANOSOL II TRU-BLU, MODEL UBL-417K041212HOUVA 3 PHOTOTHERAPY SYSTEMK982082HANDISOL WOUND HEALINGK934808UVISOL AND UVISOL IIK924969PHOTOTHERAPY TIMERK924077HANDISOL

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Related Devices (Code: KGL)

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.

K852575WALDMANN F85/100W PUVASylvania Lighting ProductsK841795UV 8001K, PUVA 800, PUVA 180/200 1000Waldmann Lighting Co.K820280SPECTRA 305/350UltraliteK810358PHOTOTHERAPY LIGHT CHAMBERPaul B. Elder Co.K791977PSORALITE MARK IPaul B. Elder Co.K791116PSORALITE SERIES 30,000Paul B. Elder Co.

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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