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FDA 510(k)

WELCH ALLYN FRONT-LINE DOC

K-Number: K984215 · 1999-02-11

ApplicantWelch Allyn, Inc.
Decision Date1999-02-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

WELCH ALLYN FRONT-LINE DOC is the device name listed in this FDA 510(k) record. The listed applicant is Welch Allyn, Inc.. It received FDA 510(k) clearance on 1999-02-11 under 510(k) number K984215. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WELCH ALLYN FRONT-LINE DOC?

WELCH ALLYN FRONT-LINE DOC is a medical device that received FDA 510(k) clearance on 1999-02-11. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K984215.

When did WELCH ALLYN FRONT-LINE DOC receive FDA 510(k) clearance?

WELCH ALLYN FRONT-LINE DOC received FDA 510(k) clearance on 1999-02-11, under 510(k) number K984215.

Who is the listed applicant for WELCH ALLYN FRONT-LINE DOC?

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

What is the FDA product code for WELCH ALLYN FRONT-LINE DOC?

The FDA product code for WELCH ALLYN FRONT-LINE DOC is LLZ.

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Other records listing Welch Allyn, Inc. as applicant

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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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