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FDA 510(k)

TONGUE BLADE HOLDER

K-Number: K771481 · 1977-08-19

ApplicantWelch Allyn, Inc.
Decision Date1977-08-19
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TONGUE BLADE HOLDER 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 1977-08-19 under 510(k) number K771481. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TONGUE BLADE HOLDER?

TONGUE BLADE HOLDER is a medical device that received FDA 510(k) clearance on 1977-08-19. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K771481.

When did TONGUE BLADE HOLDER receive FDA 510(k) clearance?

TONGUE BLADE HOLDER received FDA 510(k) clearance on 1977-08-19, under 510(k) number K771481.

Who is the listed applicant for TONGUE BLADE HOLDER?

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 TONGUE BLADE HOLDER?

The FDA product code for TONGUE BLADE HOLDER is EMA.

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Other records listing Welch Allyn, Inc. as applicant

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Related Devices (Code: EMA)

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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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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