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FDA 510(k)

SAM ST

K-Number: K913097 · 1992-12-11

Decision Date1992-12-11
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SAM ST is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1992-12-11 under 510(k) number K913097. The device is classified under product code BTI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAM ST?

SAM ST is a medical device that received FDA 510(k) clearance on 1992-12-11. The listed applicant is Ferguson Medical. The 510(k) number is K913097.

When did SAM ST receive FDA 510(k) clearance?

SAM ST received FDA 510(k) clearance on 1992-12-11, under 510(k) number K913097.

Who is the listed applicant for SAM ST?

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 SAM ST?

The FDA product code for SAM ST is BTI.

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: BTI)

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

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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