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CDS II (Sodium Chondroitin Sulfate)

by Alcon Laboratories, Inc.

PMA P820079

Withdrawn Withdrawn in United States.

Was authorized under PMA, withdrawn

Ended

Withdrawn 30 Sep 1986

PMA

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA PMA, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA PMAAPWD Approval withdrawn NumberP820079 Date30 Sep 1986Approval withdrawnStatusWithdrawn

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA PMA Withdrawn

Specification

PMA

Generic Name
AID, SURGICAL, VISCOELASTIC
FDA applicant
Alcon Laboratories
PMA Number
FDA Product Code
LZP
Device Class
Class III
Regulation
21 CFR Part 886.4275
Advisory Committee
Ophthalmic
FDA Decision
APWD Approval withdrawn

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