ABBOTT COMMANDER FLEXIBLE PIPETTING CENTER
K-Number: K894069 · 1989-08-21
Advertisement
Device Summary
Frequently Asked Questions
What is the ABBOTT COMMANDER FLEXIBLE PIPETTING CENTER?
ABBOTT COMMANDER FLEXIBLE PIPETTING CENTER is a medical device that received FDA 510(k) clearance on 1989-08-21. The listed applicant is Abbott Laboratories. The 510(k) number is K894069.
When did ABBOTT COMMANDER FLEXIBLE PIPETTING CENTER receive FDA 510(k) clearance?
ABBOTT COMMANDER FLEXIBLE PIPETTING CENTER received FDA 510(k) clearance on 1989-08-21, under 510(k) number K894069.
Who is the listed applicant for ABBOTT COMMANDER FLEXIBLE PIPETTING CENTER?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABBOTT COMMANDER FLEXIBLE PIPETTING CENTER?
The FDA product code for ABBOTT COMMANDER FLEXIBLE PIPETTING CENTER is JQW.
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 Abbott 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: JQW)
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