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FDA 510(k)

P.P.P. TREATMENT CABINET

K-Number: K813003 · 1981-11-06

ApplicantPrecision Professional Products
Decision Date1981-11-06
Product CodeERA
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

P.P.P. TREATMENT CABINET is the device name listed in this FDA 510(k) record. The listed applicant is Precision Professional Products. It received FDA 510(k) clearance on 1981-11-06 under 510(k) number K813003. The device is classified under product code ERA. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.P.P. TREATMENT CABINET?

P.P.P. TREATMENT CABINET is a medical device that received FDA 510(k) clearance on 1981-11-06. The listed applicant is Precision Professional Products. The 510(k) number is K813003.

When did P.P.P. TREATMENT CABINET receive FDA 510(k) clearance?

P.P.P. TREATMENT CABINET received FDA 510(k) clearance on 1981-11-06, under 510(k) number K813003.

Who is the listed applicant for P.P.P. TREATMENT CABINET?

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

What is the FDA product code for P.P.P. TREATMENT CABINET?

The FDA product code for P.P.P. TREATMENT CABINET is ERA.

Related Clinical Trials

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Related Devices (Code: ERA)

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.

K123821AIO HD OTOSCOPEBlue FocusK121326LANTOS 3D EAR SCANNERLantos TechnologiesK110326OSRAM ITOSOsram Sylvania, Inc.K945264OPTUS OTOSCOPESOptus, Inc.K955043WELCH ALLYN BI-OTOSCOPEWelch Allyn, Inc.K952578WELCH ALLY OTOSCOPEWelch Allyn, Inc.

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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