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FDA PMA

AID, SURGICAL, VISCOELASTIC

PMA Number: P810025 · 2023-06-22

ApplicantBausch & Lomb, Inc.
Decision Date2023-06-22
PMA NumberP810025
Product CodeLZP
Device ClassClass 3
Medical SpecialtyO
Regulation Number21 CFR 8
Advisory CommitteeOP

Device Summary

AID, SURGICAL, VISCOELASTIC is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Inc.. It received FDA 510(k) clearance on 2023-06-22. The device is classified under product code LZP. It was reviewed by the OP advisory panel.

Frequently Asked Questions

What is the AID, SURGICAL, VISCOELASTIC?

AID, SURGICAL, VISCOELASTIC is a medical device that received FDA 510(k) clearance on 2023-06-22. The listed applicant is Bausch & Lomb, Inc..

When did AID, SURGICAL, VISCOELASTIC receive FDA 510(k) clearance?

The clearance date for AID, SURGICAL, VISCOELASTIC can be found in the official FDA records.

Who is the listed applicant for AID, SURGICAL, VISCOELASTIC?

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

What is the FDA product code for AID, SURGICAL, VISCOELASTIC?

The FDA product code for AID, SURGICAL, VISCOELASTIC is LZP.

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.

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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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