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FDA 510(k)

STILLE AUTOMATIC TOURNIQUET

K-Number: K925033 · 1993-02-01

Decision Date1993-02-01
Product CodeKCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STILLE AUTOMATIC TOURNIQUET is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1993-02-01 under 510(k) number K925033. 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 STILLE AUTOMATIC TOURNIQUET?

STILLE AUTOMATIC TOURNIQUET is a medical device that received FDA 510(k) clearance on 1993-02-01. The listed applicant is Ferguson Medical. The 510(k) number is K925033.

When did STILLE AUTOMATIC TOURNIQUET receive FDA 510(k) clearance?

STILLE AUTOMATIC TOURNIQUET received FDA 510(k) clearance on 1993-02-01, under 510(k) number K925033.

Who is the listed applicant for STILLE AUTOMATIC TOURNIQUET?

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

What is the FDA product code for STILLE AUTOMATIC TOURNIQUET?

The FDA product code for STILLE AUTOMATIC 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 Ferguson Medical 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 57 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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