MODEL 807 SUCTION CAUTERY FINGER TIP
K-Number: K800022 · 1980-02-11
Advertisement
Device Summary
Frequently Asked Questions
What is the MODEL 807 SUCTION CAUTERY FINGER TIP?
MODEL 807 SUCTION CAUTERY FINGER TIP is a medical device that received FDA 510(k) clearance on 1980-02-11. The listed applicant is Malibu Laboratories. The 510(k) number is K800022.
When did MODEL 807 SUCTION CAUTERY FINGER TIP receive FDA 510(k) clearance?
MODEL 807 SUCTION CAUTERY FINGER TIP received FDA 510(k) clearance on 1980-02-11, under 510(k) number K800022.
Who is the listed applicant for MODEL 807 SUCTION CAUTERY FINGER TIP?
The FDA 510(k) record lists Malibu Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 807 SUCTION CAUTERY FINGER TIP?
The FDA product code for MODEL 807 SUCTION CAUTERY FINGER TIP is GEI.
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 Malibu Laboratories 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: GEI)
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.
Advertisement