FDA 510(k)

SAT PAD(TM)

K-Number: K926416 · 1993-05-19

Decision Date1993-05-19

Product CodeLNH

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SAT PAD(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Alliance Pharmaceutical Corp.. It received FDA 510(k) clearance on 1993-05-19 under 510(k) number K926416. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAT PAD(TM)?

SAT PAD(TM) is a medical device that received FDA 510(k) clearance on 1993-05-19. The listed applicant is Alliance Pharmaceutical Corp.. The 510(k) number is K926416.

When did SAT PAD(TM) receive FDA 510(k) clearance?

SAT PAD(TM) received FDA 510(k) clearance on 1993-05-19, under 510(k) number K926416.

Who is the listed applicant for SAT PAD(TM)?

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

What is the FDA product code for SAT PAD(TM)?

The FDA product code for SAT PAD(TM) is LNH.

Other records listing Alliance Pharmaceutical Corp. 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.

K923948SAT PAD

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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.