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FDA 510(k)

ORTHOPEDIC STOCKINETTE

K-Number: K833437 · 1983-11-03

ApplicantNorthern Medical Surgical, Inc.
Decision Date1983-11-03
Product CodeILG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ORTHOPEDIC STOCKINETTE is the device name listed in this FDA 510(k) record. The listed applicant is Northern Medical Surgical, Inc.. It received FDA 510(k) clearance on 1983-11-03 under 510(k) number K833437. 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 STOCKINETTE?

ORTHOPEDIC STOCKINETTE is a medical device that received FDA 510(k) clearance on 1983-11-03. The listed applicant is Northern Medical Surgical, Inc.. The 510(k) number is K833437.

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

ORTHOPEDIC STOCKINETTE received FDA 510(k) clearance on 1983-11-03, under 510(k) number K833437.

Who is the listed applicant for ORTHOPEDIC STOCKINETTE?

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

What is the FDA product code for ORTHOPEDIC STOCKINETTE?

The FDA product code for ORTHOPEDIC STOCKINETTE is ILG.

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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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.

K831540COMPRESSOGRIP ELASTIC STUMP SHRINKER#Fred Sammons, Inc.K780612STOCKINETTE, STERILEAbco Dealers, Inc.K780547STERILE ORTHOPEDIC STOCKINETTEAlba-Waldensian, Inc.K770346ORTHOPEDIC STOCKINETTEConvertorsK770173STOCKINETTEChase Mfg. Co.K760817ORTHOPEDIC TUBULAR STOCKINETTEParke-Davis Co.

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.

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