FDA 510(k)

STA COMPACT MAX

K-Number: K130090 · 2013-02-12

ApplicantDiagnostica Stago, Incorporated

Decision Date2013-02-12

Product CodeJPA

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

STA COMPACT MAX is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostica Stago, Incorporated. It received FDA 510(k) clearance on 2013-02-12 under 510(k) number K130090. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STA COMPACT MAX?

STA COMPACT MAX is a medical device that received FDA 510(k) clearance on 2013-02-12. The listed applicant is Diagnostica Stago, Incorporated. The 510(k) number is K130090.

When did STA COMPACT MAX receive FDA 510(k) clearance?

STA COMPACT MAX received FDA 510(k) clearance on 2013-02-12, under 510(k) number K130090.

Who is the listed applicant for STA COMPACT MAX?

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

What is the FDA product code for STA COMPACT MAX?

The FDA product code for STA COMPACT MAX is JPA.

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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.