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FDA 510(k)

BRAUN TRAVEL

K-Number: K810666 · 1981-04-14

ApplicantGilette Medical Eval. Laboratory
Decision Date1981-04-14
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BRAUN TRAVEL is the device name listed in this FDA 510(k) record. The listed applicant is Gilette Medical Eval. Laboratory. It received FDA 510(k) clearance on 1981-04-14 under 510(k) number K810666. The device is classified under product code JEQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRAUN TRAVEL?

BRAUN TRAVEL is a medical device that received FDA 510(k) clearance on 1981-04-14. The listed applicant is Gilette Medical Eval. Laboratory. The 510(k) number is K810666.

When did BRAUN TRAVEL receive FDA 510(k) clearance?

BRAUN TRAVEL received FDA 510(k) clearance on 1981-04-14, under 510(k) number K810666.

Who is the listed applicant for BRAUN TRAVEL?

The FDA 510(k) record lists Gilette Medical Eval. Laboratory as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BRAUN TRAVEL?

The FDA product code for BRAUN TRAVEL is JEQ.

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Related Devices (Code: JEQ)

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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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