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FDA 510(k)

HYPAFIX DRESSING RETENTION SHEET

K-Number: K894254 · 1989-08-31

ApplicantSmith & Nephew United, Inc.
Decision Date1989-08-31
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HYPAFIX DRESSING RETENTION SHEET is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew United, Inc.. It received FDA 510(k) clearance on 1989-08-31 under 510(k) number K894254. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYPAFIX DRESSING RETENTION SHEET?

HYPAFIX DRESSING RETENTION SHEET is a medical device that received FDA 510(k) clearance on 1989-08-31. The listed applicant is Smith & Nephew United, Inc.. The 510(k) number is K894254.

When did HYPAFIX DRESSING RETENTION SHEET receive FDA 510(k) clearance?

HYPAFIX DRESSING RETENTION SHEET received FDA 510(k) clearance on 1989-08-31, under 510(k) number K894254.

Who is the listed applicant for HYPAFIX DRESSING RETENTION SHEET?

The FDA 510(k) record lists Smith & Nephew United, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYPAFIX DRESSING RETENTION SHEET?

The FDA product code for HYPAFIX DRESSING RETENTION SHEET is NAD.

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Other records listing Smith & Nephew United, Inc. 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: NAD)

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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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