CELLIBIOSE-ARGININE-LYSINE AGAR (CAL)
K-Number: K800745 · 1980-05-02
Advertisement
Device Summary
Frequently Asked Questions
What is the CELLIBIOSE-ARGININE-LYSINE AGAR (CAL)?
CELLIBIOSE-ARGININE-LYSINE AGAR (CAL) is a medical device that received FDA 510(k) clearance on 1980-05-02. The listed applicant is Remel Co.. The 510(k) number is K800745.
When did CELLIBIOSE-ARGININE-LYSINE AGAR (CAL) receive FDA 510(k) clearance?
CELLIBIOSE-ARGININE-LYSINE AGAR (CAL) received FDA 510(k) clearance on 1980-05-02, under 510(k) number K800745.
Who is the listed applicant for CELLIBIOSE-ARGININE-LYSINE AGAR (CAL)?
The FDA 510(k) record lists Remel Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CELLIBIOSE-ARGININE-LYSINE AGAR (CAL)?
The FDA product code for CELLIBIOSE-ARGININE-LYSINE AGAR (CAL) is JSI.
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 Remel 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: 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