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)

MODEL OPO-32 IRRIGATION SLEEVE

K-Number: K874543 · 1988-01-14

Decision Date1988-01-14
Product CodeEIB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MODEL OPO-32 IRRIGATION SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Allergan, Inc.. It received FDA 510(k) clearance on 1988-01-14 under 510(k) number K874543. The device is classified under product code EIB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL OPO-32 IRRIGATION SLEEVE?

MODEL OPO-32 IRRIGATION SLEEVE is a medical device that received FDA 510(k) clearance on 1988-01-14. The listed applicant is Allergan, Inc.. The 510(k) number is K874543.

When did MODEL OPO-32 IRRIGATION SLEEVE receive FDA 510(k) clearance?

MODEL OPO-32 IRRIGATION SLEEVE received FDA 510(k) clearance on 1988-01-14, under 510(k) number K874543.

Who is the listed applicant for MODEL OPO-32 IRRIGATION SLEEVE?

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

What is the FDA product code for MODEL OPO-32 IRRIGATION SLEEVE?

The FDA product code for MODEL OPO-32 IRRIGATION SLEEVE is EIB.

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 Allergan, 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 32 devices →

Related Devices (Code: EIB)

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.

↑