ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL
K-Number: K884961 · 1989-02-13
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Device Summary
Frequently Asked Questions
What is the ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL?
ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL is a medical device that received FDA 510(k) clearance on 1989-02-13. The listed applicant is Bausch & Lomb Pharmaceutical, Inc.. The 510(k) number is K884961.
When did ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL receive FDA 510(k) clearance?
ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL received FDA 510(k) clearance on 1989-02-13, under 510(k) number K884961.
Who is the listed applicant for ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL?
The FDA 510(k) record lists Bausch & Lomb Pharmaceutical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL?
The FDA product code for ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL is MOE.
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 Bausch & Lomb Pharmaceutical, 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: MOE)
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.
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