FDA 510(k)

BURLINGTON STOCKINETTE

K-Number: K822770 · 1983-07-26

Decision Date1983-07-26

Product Code

DecisionSubstantially Equivalent

Device Summary

BURLINGTON STOCKINETTE is the device name listed in this FDA 510(k) record. The listed applicant is Balfour, Inc.. It received FDA 510(k) clearance on 1983-07-26 under 510(k) number K822770. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BURLINGTON STOCKINETTE?

BURLINGTON STOCKINETTE is a medical device that received FDA 510(k) clearance on 1983-07-26. The listed applicant is Balfour, Inc.. The 510(k) number is K822770.

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

BURLINGTON STOCKINETTE received FDA 510(k) clearance on 1983-07-26, under 510(k) number K822770.

Who is the listed applicant for BURLINGTON STOCKINETTE?

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

Related Clinical Trials

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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Other records listing Balfour, Inc. as applicant

K833121BURLINGTON STERILE ANTIMICROBIAL STOCK K833122BURLINGTON ANTIMICROBIAL STOCKINEETTE

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.