PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST
K-Number: K882223 · 1988-08-16
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Device Summary
Frequently Asked Questions
What is the PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST?
PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST is a medical device that received FDA 510(k) clearance on 1988-08-16. The listed applicant is Deknatel, Inc.. The 510(k) number is K882223.
When did PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST receive FDA 510(k) clearance?
PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST received FDA 510(k) clearance on 1988-08-16, under 510(k) number K882223.
Who is the listed applicant for PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST?
The FDA 510(k) record lists Deknatel, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST?
The FDA product code for PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST 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 Deknatel, 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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