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FDA 510(k)

STERILE IMPERVIOUS ORTHOPEDIC STOCKINETTE

K-Number: K941302 · 1994-05-12

ApplicantCush Industries, Inc.
Decision Date1994-05-12
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE IMPERVIOUS ORTHOPEDIC STOCKINETTE is the device name listed in this FDA 510(k) record. The listed applicant is Cush Industries, Inc.. It received FDA 510(k) clearance on 1994-05-12 under 510(k) number K941302. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE IMPERVIOUS ORTHOPEDIC STOCKINETTE?

STERILE IMPERVIOUS ORTHOPEDIC STOCKINETTE is a medical device that received FDA 510(k) clearance on 1994-05-12. The listed applicant is Cush Industries, Inc.. The 510(k) number is K941302.

When did STERILE IMPERVIOUS ORTHOPEDIC STOCKINETTE receive FDA 510(k) clearance?

STERILE IMPERVIOUS ORTHOPEDIC STOCKINETTE received FDA 510(k) clearance on 1994-05-12, under 510(k) number K941302.

Who is the listed applicant for STERILE IMPERVIOUS ORTHOPEDIC STOCKINETTE?

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

What is the FDA product code for STERILE IMPERVIOUS ORTHOPEDIC STOCKINETTE?

The FDA product code for STERILE IMPERVIOUS ORTHOPEDIC STOCKINETTE is KKX.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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