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FDA 510(k)

STERILE TUBULAR UNBLEACHED STOCKINETTE

K-Number: K760750 · 1976-10-08

ApplicantDennison Manufacturing Co.
Decision Date1976-10-08
Product CodeJLG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

STERILE TUBULAR UNBLEACHED STOCKINETTE is the device name listed in this FDA 510(k) record. The listed applicant is Dennison Manufacturing Co.. It received FDA 510(k) clearance on 1976-10-08 under 510(k) number K760750. The device is classified under product code JLG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE TUBULAR UNBLEACHED STOCKINETTE?

STERILE TUBULAR UNBLEACHED STOCKINETTE is a medical device that received FDA 510(k) clearance on 1976-10-08. The listed applicant is Dennison Manufacturing Co.. The 510(k) number is K760750.

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

STERILE TUBULAR UNBLEACHED STOCKINETTE received FDA 510(k) clearance on 1976-10-08, under 510(k) number K760750.

Who is the listed applicant for STERILE TUBULAR UNBLEACHED STOCKINETTE?

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

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

The FDA product code for STERILE TUBULAR UNBLEACHED STOCKINETTE is JLG.

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Related Devices (Code: JLG)

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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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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