FDA 510(k)

SET PP

K-Number: K073043 · 2007-12-14

Decision Date2007-12-14

Product CodeEMA

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

SET PP is the device name listed in this FDA 510(k) record. The listed applicant is Sdi , Ltd.. It received FDA 510(k) clearance on 2007-12-14 under 510(k) number K073043. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SET PP?

SET PP is a medical device that received FDA 510(k) clearance on 2007-12-14. The listed applicant is Sdi , Ltd.. The 510(k) number is K073043.

When did SET PP receive FDA 510(k) clearance?

SET PP received FDA 510(k) clearance on 2007-12-14, under 510(k) number K073043.

Who is the listed applicant for SET PP?

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

What is the FDA product code for SET PP?

The FDA product code for SET PP is EMA.

Other records listing Sdi , Ltd. 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.

K081273ULTRACAPS S

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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.