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FDA 510(k)

DPA 207 PERSONAL

K-Number: K802513 · 1980-12-16

ApplicantHill, Farrer & Borrill
Decision Date1980-12-16
Product CodeKCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DPA 207 PERSONAL is the device name listed in this FDA 510(k) record. The listed applicant is Hill, Farrer & Borrill. It received FDA 510(k) clearance on 1980-12-16 under 510(k) number K802513. The device is classified under product code KCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DPA 207 PERSONAL?

DPA 207 PERSONAL is a medical device that received FDA 510(k) clearance on 1980-12-16. The listed applicant is Hill, Farrer & Borrill. The 510(k) number is K802513.

When did DPA 207 PERSONAL receive FDA 510(k) clearance?

DPA 207 PERSONAL received FDA 510(k) clearance on 1980-12-16, under 510(k) number K802513.

Who is the listed applicant for DPA 207 PERSONAL?

The FDA 510(k) record lists Hill, Farrer & Borrill as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DPA 207 PERSONAL?

The FDA product code for DPA 207 PERSONAL is KCX.

Related Clinical Trials

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Related Devices (Code: KCX)

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.

K973773DAPELLE HAIR REMOVERWellquest Intl., Inc.K973340TWEEZER-TYPE EPILATORMobit, Inc.K973179FEMINIQUE SONIC HAIR REMOVERGlobal TV Concepts, Ltd.K973174SONIQUE HAIR REMOVERGlobal TV Concepts, Ltd.K972695FINALLY FREEMehl/Group MarketingK970338TWEEZER-TYPE EPILATORIgia Direct, Inc.

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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