GENERAL PURPOSE CENTRIFUGE
K-Number: K864974 · 1987-01-09
Advertisement
Device Summary
Frequently Asked Questions
What is the GENERAL PURPOSE CENTRIFUGE?
GENERAL PURPOSE CENTRIFUGE is a medical device that received FDA 510(k) clearance on 1987-01-09. The listed applicant is Norfolk Scientific, Inc.. The 510(k) number is K864974.
When did GENERAL PURPOSE CENTRIFUGE receive FDA 510(k) clearance?
GENERAL PURPOSE CENTRIFUGE received FDA 510(k) clearance on 1987-01-09, under 510(k) number K864974.
Who is the listed applicant for GENERAL PURPOSE CENTRIFUGE?
The FDA 510(k) record lists Norfolk Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GENERAL PURPOSE CENTRIFUGE?
The FDA product code for GENERAL PURPOSE CENTRIFUGE is JQC.
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 Norfolk Scientific, 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: JQC)
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