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FDA 510(k)

ORTHOPEDIC TUBULAR STOCKINETTE

K-Number: K760817 · 1976-10-20

ApplicantParke-Davis Co.
Decision Date1976-10-20
Product CodeILG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ORTHOPEDIC TUBULAR STOCKINETTE is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1976-10-20 under 510(k) number K760817. The device is classified under product code ILG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOPEDIC TUBULAR STOCKINETTE?

ORTHOPEDIC TUBULAR STOCKINETTE is a medical device that received FDA 510(k) clearance on 1976-10-20. The listed applicant is Parke-Davis Co.. The 510(k) number is K760817.

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

ORTHOPEDIC TUBULAR STOCKINETTE received FDA 510(k) clearance on 1976-10-20, under 510(k) number K760817.

Who is the listed applicant for ORTHOPEDIC TUBULAR STOCKINETTE?

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

What is the FDA product code for ORTHOPEDIC TUBULAR STOCKINETTE?

The FDA product code for ORTHOPEDIC TUBULAR STOCKINETTE is ILG.

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Related Devices (Code: ILG)

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.

K833437ORTHOPEDIC STOCKINETTENorthern Medical Surgical, Inc.K831540COMPRESSOGRIP ELASTIC STUMP SHRINKER#Fred Sammons, Inc.K780612STOCKINETTE, STERILEAbco Dealers, Inc.K780547STERILE ORTHOPEDIC STOCKINETTEAlba-Waldensian, Inc.K770346ORTHOPEDIC STOCKINETTEConvertorsK770173STOCKINETTEChase Mfg. Co.

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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