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FDA 510(k)

A.T.S. 1500 TOURNIQUET

K-Number: K870784 · 1987-03-18

Decision Date1987-03-18
Product CodeKCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

A.T.S. 1500 TOURNIQUET is the device name listed in this FDA 510(k) record. The listed applicant is Aspen Laboratories, Inc.. It received FDA 510(k) clearance on 1987-03-18 under 510(k) number K870784. The device is classified under product code KCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A.T.S. 1500 TOURNIQUET?

A.T.S. 1500 TOURNIQUET is a medical device that received FDA 510(k) clearance on 1987-03-18. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K870784.

When did A.T.S. 1500 TOURNIQUET receive FDA 510(k) clearance?

A.T.S. 1500 TOURNIQUET received FDA 510(k) clearance on 1987-03-18, under 510(k) number K870784.

Who is the listed applicant for A.T.S. 1500 TOURNIQUET?

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

What is the FDA product code for A.T.S. 1500 TOURNIQUET?

The FDA product code for A.T.S. 1500 TOURNIQUET is KCY.

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 Aspen Laboratories, 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.

View all 55 devices →

Related Devices (Code: KCY)

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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