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FDA 510(k)

THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEM

K-Number: K897057 · 1990-03-16

Decision Date1990-03-16
Product CodeBYH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEM 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 1990-03-16 under 510(k) number K897057. 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 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.

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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