CHONDROITIN SULFATE CORNEAL STORAGE MEDIUM
K-Number: K870251 · 1987-04-06
Advertisement
Device Summary
Frequently Asked Questions
What is the CHONDROITIN SULFATE CORNEAL STORAGE MEDIUM?
CHONDROITIN SULFATE CORNEAL STORAGE MEDIUM is a medical device that received FDA 510(k) clearance on 1987-04-06. The listed applicant is Bioclinical Laboratory Services, Inc.. The 510(k) number is K870251.
When did CHONDROITIN SULFATE CORNEAL STORAGE MEDIUM receive FDA 510(k) clearance?
CHONDROITIN SULFATE CORNEAL STORAGE MEDIUM received FDA 510(k) clearance on 1987-04-06, under 510(k) number K870251.
Who is the listed applicant for CHONDROITIN SULFATE CORNEAL STORAGE MEDIUM?
The FDA 510(k) record lists Bioclinical Laboratory Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHONDROITIN SULFATE CORNEAL STORAGE MEDIUM?
The FDA product code for CHONDROITIN SULFATE CORNEAL STORAGE MEDIUM is LYX.
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 Bioclinical Laboratory Services, 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: LYX)
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