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)

SURGICAL INSTRUMENTS, OPTHALMIC

K-Number: K760326 · 1976-08-04

ApplicantDepuy, Inc.
Decision Date1976-08-04
Product CodeHNF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SURGICAL INSTRUMENTS, OPTHALMIC is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1976-08-04 under 510(k) number K760326. The device is classified under product code HNF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL INSTRUMENTS, OPTHALMIC?

SURGICAL INSTRUMENTS, OPTHALMIC is a medical device that received FDA 510(k) clearance on 1976-08-04. The listed applicant is Depuy, Inc.. The 510(k) number is K760326.

When did SURGICAL INSTRUMENTS, OPTHALMIC receive FDA 510(k) clearance?

SURGICAL INSTRUMENTS, OPTHALMIC received FDA 510(k) clearance on 1976-08-04, under 510(k) number K760326.

Who is the listed applicant for SURGICAL INSTRUMENTS, OPTHALMIC?

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

What is the FDA product code for SURGICAL INSTRUMENTS, OPTHALMIC?

The FDA product code for SURGICAL INSTRUMENTS, OPTHALMIC is HNF.

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 Depuy, 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 303 devices →

Related Devices (Code: HNF)

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.

↑