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FDA 510(k)

ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL

K-Number: K884961 · 1989-02-13

Decision Date1989-02-13
Product CodeMOE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb Pharmaceutical, Inc.. It received FDA 510(k) clearance on 1989-02-13 under 510(k) number K884961. The device is classified under product code MOE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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