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FDA 510(k)

STASILON FR

K-Number: K072890 · 2007-12-10

ApplicantEntegrion, Inc.
Decision Date2007-12-10
Product CodeQSY
DecisionSubstantially Equivalent

Device Summary

STASILON FR is the device name listed in this FDA 510(k) record. The listed applicant is Entegrion, Inc.. It received FDA 510(k) clearance on 2007-12-10 under 510(k) number K072890. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STASILON FR?

STASILON FR is a medical device that received FDA 510(k) clearance on 2007-12-10. The listed applicant is Entegrion, Inc.. The 510(k) number is K072890.

When did STASILON FR receive FDA 510(k) clearance?

STASILON FR received FDA 510(k) clearance on 2007-12-10, under 510(k) number K072890.

Who is the listed applicant for STASILON FR?

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

What is the FDA product code for STASILON FR?

The FDA product code for STASILON FR is QSY.

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Related Devices (Code: QSY)

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.

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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.

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