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FDA 510(k)

BRAUN THERMOSCAN PRO3000 INFARED THERMOMETER

K-Number: K992468 · 1999-10-20

ApplicantBraun GmbH
Decision Date1999-10-20
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BRAUN THERMOSCAN PRO3000 INFARED THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Braun GmbH. It received FDA 510(k) clearance on 1999-10-20 under 510(k) number K992468. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRAUN THERMOSCAN PRO3000 INFARED THERMOMETER?

BRAUN THERMOSCAN PRO3000 INFARED THERMOMETER is a medical device that received FDA 510(k) clearance on 1999-10-20. The listed applicant is Braun GmbH. The 510(k) number is K992468.

When did BRAUN THERMOSCAN PRO3000 INFARED THERMOMETER receive FDA 510(k) clearance?

BRAUN THERMOSCAN PRO3000 INFARED THERMOMETER received FDA 510(k) clearance on 1999-10-20, under 510(k) number K992468.

Who is the listed applicant for BRAUN THERMOSCAN PRO3000 INFARED THERMOMETER?

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

What is the FDA product code for BRAUN THERMOSCAN PRO3000 INFARED THERMOMETER?

The FDA product code for BRAUN THERMOSCAN PRO3000 INFARED THERMOMETER is FLL.

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.

Other records listing Braun GmbH 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.

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Related Devices (Code: FLL)

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.

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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