LUNG FORCEPS
K-Number: K890262 · 1989-01-27
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Device Summary
Frequently Asked Questions
What is the LUNG FORCEPS?
LUNG FORCEPS is a medical device that received FDA 510(k) clearance on 1989-01-27. The listed applicant is Kinetic Medical Products. The 510(k) number is K890262.
When did LUNG FORCEPS receive FDA 510(k) clearance?
LUNG FORCEPS received FDA 510(k) clearance on 1989-01-27, under 510(k) number K890262.
Who is the listed applicant for LUNG FORCEPS?
The FDA 510(k) record lists Kinetic Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUNG FORCEPS?
The FDA product code for LUNG FORCEPS is HTD.
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 Kinetic Medical Products 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: HTD)
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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