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FDA 510(k)

THAYER SUCTION EVACUATION CONDENSATE COLLECTION

K-Number: K900047 · 1990-04-23

Decision Date1990-04-23
Product CodeBYH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THAYER SUCTION EVACUATION CONDENSATE COLLECTION is the device name listed in this FDA 510(k) record. The listed applicant is Thayer Medical Corp.. It received FDA 510(k) clearance on 1990-04-23 under 510(k) number K900047. The device is classified under product code BYH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THAYER SUCTION EVACUATION CONDENSATE COLLECTION?

THAYER SUCTION EVACUATION CONDENSATE COLLECTION is a medical device that received FDA 510(k) clearance on 1990-04-23. The listed applicant is Thayer Medical Corp.. The 510(k) number is K900047.

When did THAYER SUCTION EVACUATION CONDENSATE COLLECTION receive FDA 510(k) clearance?

THAYER SUCTION EVACUATION CONDENSATE COLLECTION received FDA 510(k) clearance on 1990-04-23, under 510(k) number K900047.

Who is the listed applicant for THAYER SUCTION EVACUATION CONDENSATE COLLECTION?

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

What is the FDA product code for THAYER SUCTION EVACUATION CONDENSATE COLLECTION?

The FDA product code for THAYER SUCTION EVACUATION CONDENSATE COLLECTION is BYH.

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 Thayer Medical 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.

View all 15 devices →

Related Devices (Code: BYH)

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

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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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