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FDA 510(k)

TUBULAR DRESSING RETAINER

K-Number: K780570 · 1978-04-19

ApplicantAlba-Waldensian, Inc.
Decision Date1978-04-19
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TUBULAR DRESSING RETAINER is the device name listed in this FDA 510(k) record. The listed applicant is Alba-Waldensian, Inc.. It received FDA 510(k) clearance on 1978-04-19 under 510(k) number K780570. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBULAR DRESSING RETAINER?

TUBULAR DRESSING RETAINER is a medical device that received FDA 510(k) clearance on 1978-04-19. The listed applicant is Alba-Waldensian, Inc.. The 510(k) number is K780570.

When did TUBULAR DRESSING RETAINER receive FDA 510(k) clearance?

TUBULAR DRESSING RETAINER received FDA 510(k) clearance on 1978-04-19, under 510(k) number K780570.

Who is the listed applicant for TUBULAR DRESSING RETAINER?

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

What is the FDA product code for TUBULAR DRESSING RETAINER?

The FDA product code for TUBULAR DRESSING RETAINER is FQM.

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Other records listing Alba-Waldensian, 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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