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FDA 510(k)

STERILE STOCKINETTE

K-Number: K760867 · 1976-11-03

ApplicantAbco Dealers, Inc.
Decision Date1976-11-03
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE STOCKINETTE is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1976-11-03 under 510(k) number K760867. 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 STOCKINETTE?

STERILE STOCKINETTE is a medical device that received FDA 510(k) clearance on 1976-11-03. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K760867.

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

STERILE STOCKINETTE received FDA 510(k) clearance on 1976-11-03, under 510(k) number K760867.

Who is the listed applicant for STERILE STOCKINETTE?

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

What is the FDA product code for STERILE STOCKINETTE?

The FDA product code for STERILE STOCKINETTE is KKX.

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Other records listing Abco Dealers, 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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