THORA-KLEX CHEST DRAINAGE UNIT
K-Number: K896127 · 1990-01-24
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Device Summary
Frequently Asked Questions
What is the THORA-KLEX CHEST DRAINAGE UNIT?
THORA-KLEX CHEST DRAINAGE UNIT is a medical device that received FDA 510(k) clearance on 1990-01-24. The listed applicant is Davol, Inc.. The 510(k) number is K896127.
When did THORA-KLEX CHEST DRAINAGE UNIT receive FDA 510(k) clearance?
THORA-KLEX CHEST DRAINAGE UNIT received FDA 510(k) clearance on 1990-01-24, under 510(k) number K896127.
Who is the listed applicant for THORA-KLEX CHEST DRAINAGE UNIT?
The FDA 510(k) record lists Davol, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THORA-KLEX CHEST DRAINAGE UNIT?
The FDA product code for THORA-KLEX CHEST DRAINAGE UNIT is KDQ.
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 Davol, 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.
Related Devices (Code: KDQ)
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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