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FDA 510(k)

DERMALIGHT PSORACOMB

K-Number: K903660 · 1991-07-17

ApplicantSolitec GmbH
Decision Date1991-07-17
Product CodeIOB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DERMALIGHT PSORACOMB is the device name listed in this FDA 510(k) record. The listed applicant is Solitec GmbH. It received FDA 510(k) clearance on 1991-07-17 under 510(k) number K903660. The device is classified under product code IOB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMALIGHT PSORACOMB?

DERMALIGHT PSORACOMB is a medical device that received FDA 510(k) clearance on 1991-07-17. The listed applicant is Solitec GmbH. The 510(k) number is K903660.

When did DERMALIGHT PSORACOMB receive FDA 510(k) clearance?

DERMALIGHT PSORACOMB received FDA 510(k) clearance on 1991-07-17, under 510(k) number K903660.

Who is the listed applicant for DERMALIGHT PSORACOMB?

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

What is the FDA product code for DERMALIGHT PSORACOMB?

The FDA product code for DERMALIGHT PSORACOMB is IOB.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Solitec GmbH 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.

K828671UVATEC SUNTAMED 4000 AND 2000K828670UVATEC SUNTAMED 400

Related Devices (Code: IOB)

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.

K910091ULTRALITE PANELITEUltraliteK842276SUNMASTERMt. Hood Mfr., Inc.K813451UVA FLUORESCENT TANNING LAMPSNorth American Philips Corp.K812853OSRAM UVA LAMPOsram GmbHK760519SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313Dermatron Corp.

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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