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FDA 510(k)

ALCON SURGICAL PROCEDURE PACKS

K-Number: K880961 · 1988-04-29

Decision Date1988-04-29
Product CodeLRO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ALCON SURGICAL PROCEDURE PACKS is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1988-04-29 under 510(k) number K880961. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALCON SURGICAL PROCEDURE PACKS?

ALCON SURGICAL PROCEDURE PACKS is a medical device that received FDA 510(k) clearance on 1988-04-29. The listed applicant is Alcon Laboratories. The 510(k) number is K880961.

When did ALCON SURGICAL PROCEDURE PACKS receive FDA 510(k) clearance?

ALCON SURGICAL PROCEDURE PACKS received FDA 510(k) clearance on 1988-04-29, under 510(k) number K880961.

Who is the listed applicant for ALCON SURGICAL PROCEDURE PACKS?

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

What is the FDA product code for ALCON SURGICAL PROCEDURE PACKS?

The FDA product code for ALCON SURGICAL PROCEDURE PACKS is LRO.

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 Alcon Laboratories 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 47 devices →

Related Devices (Code: LRO)

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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