THAYER SUCTION EVACUATION CONDENSATE COLLECTION
K-Number: K900047 · 1990-04-23
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Device Summary
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.
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
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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