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FDA 510(k)

SUNMASTER

K-Number: K842276 · 1984-07-16

ApplicantMt. Hood Mfr., Inc.
Decision Date1984-07-16
Product CodeIOB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SUNMASTER is the device name listed in this FDA 510(k) record. The listed applicant is Mt. Hood Mfr., Inc.. It received FDA 510(k) clearance on 1984-07-16 under 510(k) number K842276. 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 SUNMASTER?

SUNMASTER is a medical device that received FDA 510(k) clearance on 1984-07-16. The listed applicant is Mt. Hood Mfr., Inc.. The 510(k) number is K842276.

When did SUNMASTER receive FDA 510(k) clearance?

SUNMASTER received FDA 510(k) clearance on 1984-07-16, under 510(k) number K842276.

Who is the listed applicant for SUNMASTER?

The FDA 510(k) record lists Mt. Hood Mfr., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNMASTER?

The FDA product code for SUNMASTER is IOB.

Related Clinical Trials

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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 PANELITEUltraliteK813451UVA FLUORESCENT TANNING LAMPSNorth American Philips Corp.K812853OSRAM UVA LAMPOsram GmbHK760519SUNLAMP, 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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