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FDA 510(k)

WALDMANN F85/100W PUVA

K-Number: K852575 · 1985-08-16

ApplicantSylvania Lighting Products
Decision Date1985-08-16
Product CodeKGL
Advisory CommitteeSU
DecisionUnknown

Device Summary

WALDMANN F85/100W PUVA is the device name listed in this FDA 510(k) record. The listed applicant is Sylvania Lighting Products. It received FDA 510(k) clearance on 1985-08-16 under 510(k) number K852575. The device is classified under product code KGL. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the WALDMANN F85/100W PUVA?

WALDMANN F85/100W PUVA is a medical device that received FDA 510(k) clearance on 1985-08-16. The listed applicant is Sylvania Lighting Products. The 510(k) number is K852575.

When did WALDMANN F85/100W PUVA receive FDA 510(k) clearance?

WALDMANN F85/100W PUVA received FDA 510(k) clearance on 1985-08-16, under 510(k) number K852575.

Who is the listed applicant for WALDMANN F85/100W PUVA?

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

What is the FDA product code for WALDMANN F85/100W PUVA?

The FDA product code for WALDMANN F85/100W PUVA is KGL.

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.

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Other records listing Sylvania Lighting Products 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.

K852684WALDMANN F85/100W UV21K852321SYLVANIA F8T5/PUVA & WALDMANN F15T8/PUVAK852576WALDMANN F85/100W UV6

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.

K841795UV 8001K, PUVA 800, PUVA 180/200 1000Waldmann Lighting Co.K820280SPECTRA 305/350UltraliteK810668HO-B-LITE VI UNITNational Biological Corp.K810358PHOTOTHERAPY 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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