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FDA 510(k)

COMPRESSION LEGGING DEVICE

K-Number: K871889 · 1987-08-04

Decision Date1987-08-04
Product CodeLLK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COMPRESSION LEGGING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is A-T Surgical Mfg. Co., Inc.. It received FDA 510(k) clearance on 1987-08-04 under 510(k) number K871889. The device is classified under product code LLK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPRESSION LEGGING DEVICE?

COMPRESSION LEGGING DEVICE is a medical device that received FDA 510(k) clearance on 1987-08-04. The listed applicant is A-T Surgical Mfg. Co., Inc.. The 510(k) number is K871889.

When did COMPRESSION LEGGING DEVICE receive FDA 510(k) clearance?

COMPRESSION LEGGING DEVICE received FDA 510(k) clearance on 1987-08-04, under 510(k) number K871889.

Who is the listed applicant for COMPRESSION LEGGING DEVICE?

The FDA 510(k) record lists A-T Surgical Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPRESSION LEGGING DEVICE?

The FDA product code for COMPRESSION LEGGING DEVICE is LLK.

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.

Other records listing A-T Surgical Mfg. Co., Inc. as applicant

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.

Related Devices (Code: LLK)

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.

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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