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FDA 510(k)

STOCKINETTE, TUBULAR UNBLEACHED

K-Number: K790210 · 1979-02-27

ApplicantThe Owenby Co.
Decision Date1979-02-27
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STOCKINETTE, TUBULAR UNBLEACHED is the device name listed in this FDA 510(k) record. The listed applicant is The Owenby Co.. It received FDA 510(k) clearance on 1979-02-27 under 510(k) number K790210. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STOCKINETTE, TUBULAR UNBLEACHED?

STOCKINETTE, TUBULAR UNBLEACHED is a medical device that received FDA 510(k) clearance on 1979-02-27. The listed applicant is The Owenby Co.. The 510(k) number is K790210.

When did STOCKINETTE, TUBULAR UNBLEACHED receive FDA 510(k) clearance?

STOCKINETTE, TUBULAR UNBLEACHED received FDA 510(k) clearance on 1979-02-27, under 510(k) number K790210.

Who is the listed applicant for STOCKINETTE, TUBULAR UNBLEACHED?

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

What is the FDA product code for STOCKINETTE, TUBULAR UNBLEACHED?

The FDA product code for STOCKINETTE, TUBULAR UNBLEACHED is FQM.

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Other records listing The Owenby Co. as applicant

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Related Devices (Code: FQM)

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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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