Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BARNES-HIND ROSE BENGAL OPHTHALMIC STR.

K-Number: K810285 · 1981-04-17

Decision Date1981-04-17
Product CodeKYC
DecisionSubstantially Equivalent

Device Summary

BARNES-HIND ROSE BENGAL OPHTHALMIC STR. is the device name listed in this FDA 510(k) record. The listed applicant is Barnes-Hind, Inc.. It received FDA 510(k) clearance on 1981-04-17 under 510(k) number K810285. The device is classified under product code KYC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARNES-HIND ROSE BENGAL OPHTHALMIC STR.?

BARNES-HIND ROSE BENGAL OPHTHALMIC STR. is a medical device that received FDA 510(k) clearance on 1981-04-17. The listed applicant is Barnes-Hind, Inc.. The 510(k) number is K810285.

When did BARNES-HIND ROSE BENGAL OPHTHALMIC STR. receive FDA 510(k) clearance?

BARNES-HIND ROSE BENGAL OPHTHALMIC STR. received FDA 510(k) clearance on 1981-04-17, under 510(k) number K810285.

Who is the listed applicant for BARNES-HIND ROSE BENGAL OPHTHALMIC STR.?

The FDA 510(k) record lists Barnes-Hind, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARNES-HIND ROSE BENGAL OPHTHALMIC STR.?

The FDA product code for BARNES-HIND ROSE BENGAL OPHTHALMIC STR. is KYC.

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 Barnes-Hind, 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.

View all 7 devices →

Related Devices (Code: KYC)

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.

↑