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FDA 510(k)

AQUAPLAST TIE DOWN DRESSING

K-Number: K943871 · 1994-09-30

ApplicantWfr/Aquaplast Corp.
Decision Date1994-09-30
Product CodeLZM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AQUAPLAST TIE DOWN DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Wfr/Aquaplast Corp.. It received FDA 510(k) clearance on 1994-09-30 under 510(k) number K943871. The device is classified under product code LZM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUAPLAST TIE DOWN DRESSING?

AQUAPLAST TIE DOWN DRESSING is a medical device that received FDA 510(k) clearance on 1994-09-30. The listed applicant is Wfr/Aquaplast Corp.. The 510(k) number is K943871.

When did AQUAPLAST TIE DOWN DRESSING receive FDA 510(k) clearance?

AQUAPLAST TIE DOWN DRESSING received FDA 510(k) clearance on 1994-09-30, under 510(k) number K943871.

Who is the listed applicant for AQUAPLAST TIE DOWN DRESSING?

The FDA 510(k) record lists Wfr/Aquaplast Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AQUAPLAST TIE DOWN DRESSING?

The FDA product code for AQUAPLAST TIE DOWN DRESSING is LZM.

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Other records listing Wfr/Aquaplast Corp. as applicant

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Related Devices (Code: LZM)

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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