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FDA 510(k)

OSRAM UVA LAMP

K-Number: K812853 · 1981-12-09

ApplicantOsram GmbH
Decision Date1981-12-09
Product CodeIOB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

OSRAM UVA LAMP is the device name listed in this FDA 510(k) record. The listed applicant is Osram GmbH. It received FDA 510(k) clearance on 1981-12-09 under 510(k) number K812853. 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 OSRAM UVA LAMP?

OSRAM UVA LAMP is a medical device that received FDA 510(k) clearance on 1981-12-09. The listed applicant is Osram GmbH. The 510(k) number is K812853.

When did OSRAM UVA LAMP receive FDA 510(k) clearance?

OSRAM UVA LAMP received FDA 510(k) clearance on 1981-12-09, under 510(k) number K812853.

Who is the listed applicant for OSRAM UVA LAMP?

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

What is the FDA product code for OSRAM UVA LAMP?

The FDA product code for OSRAM UVA LAMP 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 Osram 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.

K863937OSRAM ULTRAMED 400 W

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.

K903660DERMALIGHT PSORACOMBSolitec GmbHK910091ULTRALITE PANELITEUltraliteK842276SUNMASTERMt. Hood Mfr., Inc.K813451UVA FLUORESCENT TANNING LAMPSNorth American Philips Corp.K760519SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313Dermatron Corp.

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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