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FDA 510(k)

BROWNIE BOOTH BB1

K-Number: K842975 · 1984-08-17

ApplicantWeingart, Inc.
Decision Date1984-08-17
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BROWNIE BOOTH BB1 is the device name listed in this FDA 510(k) record. The listed applicant is Weingart, Inc.. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K842975. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BROWNIE BOOTH BB1?

BROWNIE BOOTH BB1 is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Weingart, Inc.. The 510(k) number is K842975.

When did BROWNIE BOOTH BB1 receive FDA 510(k) clearance?

BROWNIE BOOTH BB1 received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842975.

Who is the listed applicant for BROWNIE BOOTH BB1?

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

What is the FDA product code for BROWNIE BOOTH BB1?

The FDA product code for BROWNIE BOOTH BB1 is FTC.

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 Weingart, Inc. 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.

K863518WEINGART MODEL 1000 SUNLAMP PRODUCTK842379ELECTRO-SAGE MODEL 203

Related Devices (Code: FTC)

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.

K254234Phototherapy System (DUV-COMBO)Choyang Medics Co., Ltd.K253871Klär Lite (RCW-KL1000)Radcliffe Watts, LLCK250425Ultraviolet Phototherapy DeviceAPK Technology Co., Ltd.K244022308nm UV Phototherapy System (UV-K); 308nm UV Phototherapy System (UV-X); 308nm UV Phototherapy System (UV-Y); 308nm UV Phototherapy System (UV-Z)Boston Aesthetics, Inc.K242977308nm Excimer Phototherapy Device (CN-308E, KN-4003B3, KN-4003B4, KN-5000C KN-5000D, KN-5000H, KN-5000K)Xuzhou Kernel Medical Equipment Co., Ltd.K242908UV Phototherapy Device (Group A: SQ308PCHFD, SQ308PCQFD, SQ308PCPFD, SQ308PCNFD, SQ308PCMFD); UV Phototherapy Device (Group B: SQ308PHTFF, SQ308PHSFF, SQ308PHRFF, SQ308PHZFG, SQ308PPUFF, SQ308PPVFF, SQ308PPWFG)Shanghai Sigma High-Tech Co., Ltd.

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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