THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEM
K-Number: K897057 · 1990-03-16
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Device Summary
Frequently Asked Questions
What is the THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEM?
THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEM is a medical device that received FDA 510(k) clearance on 1990-03-16. The listed applicant is Thayer Medical Corp.. The 510(k) number is K897057.
When did THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEM receive FDA 510(k) clearance?
THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEM received FDA 510(k) clearance on 1990-03-16, under 510(k) number K897057.
Who is the listed applicant for THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEM?
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 SEMI-RIGID CONDENSATE COLLECTION SYSTEM?
The FDA product code for THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEM 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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