BLUE AGAR
K-Number: K832618 · 1983-09-12
Advertisement
Device Summary
Frequently Asked Questions
What is the BLUE AGAR?
BLUE AGAR is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Carroll Biological Corp.. The 510(k) number is K832618.
When did BLUE AGAR receive FDA 510(k) clearance?
BLUE AGAR received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832618.
Who is the listed applicant for BLUE AGAR?
The FDA 510(k) record lists Carroll Biological Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLUE AGAR?
The FDA product code for BLUE AGAR is JSI.
Other records listing Carroll Biological Corp. 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: JSI)
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