IRON & MAGNESIUM ADDITIONS/REFERRIL B CALIBRATOR
K-Number: K871664 · 1987-05-08
Advertisement
Device Summary
Frequently Asked Questions
What is the IRON & MAGNESIUM ADDITIONS/REFERRIL B CALIBRATOR?
IRON & MAGNESIUM ADDITIONS/REFERRIL B CALIBRATOR is a medical device that received FDA 510(k) clearance on 1987-05-08. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K871664.
When did IRON & MAGNESIUM ADDITIONS/REFERRIL B CALIBRATOR receive FDA 510(k) clearance?
IRON & MAGNESIUM ADDITIONS/REFERRIL B CALIBRATOR received FDA 510(k) clearance on 1987-05-08, under 510(k) number K871664.
Who is the listed applicant for IRON & MAGNESIUM ADDITIONS/REFERRIL B CALIBRATOR?
The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IRON & MAGNESIUM ADDITIONS/REFERRIL B CALIBRATOR?
The FDA product code for IRON & MAGNESIUM ADDITIONS/REFERRIL B CALIBRATOR is JIX.
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 Instrumentation Laboratory CO 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: JIX)
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