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FDA 510(k)

DEFENDO DISPOSABLE SUCTION VALVE MODEL 100305

K-Number: K102581 · 2010-11-08

Decision Date2010-11-08
Product CodeODC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DEFENDO DISPOSABLE SUCTION VALVE MODEL 100305 is the device name listed in this FDA 510(k) record. The listed applicant is Byrne Medical, Inc.. It received FDA 510(k) clearance on 2010-11-08 under 510(k) number K102581. The device is classified under product code ODC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEFENDO DISPOSABLE SUCTION VALVE MODEL 100305?

DEFENDO DISPOSABLE SUCTION VALVE MODEL 100305 is a medical device that received FDA 510(k) clearance on 2010-11-08. The listed applicant is Byrne Medical, Inc.. The 510(k) number is K102581.

When did DEFENDO DISPOSABLE SUCTION VALVE MODEL 100305 receive FDA 510(k) clearance?

DEFENDO DISPOSABLE SUCTION VALVE MODEL 100305 received FDA 510(k) clearance on 2010-11-08, under 510(k) number K102581.

Who is the listed applicant for DEFENDO DISPOSABLE SUCTION VALVE MODEL 100305?

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

What is the FDA product code for DEFENDO DISPOSABLE SUCTION VALVE MODEL 100305?

The FDA product code for DEFENDO DISPOSABLE SUCTION VALVE MODEL 100305 is ODC.

Related Clinical Trials

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.

Other records listing Byrne Medical, Inc. 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 12 devices →

Related Devices (Code: ODC)

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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