SODIUM CHLORIDE TABLETS, USP

FDA Premarket Approval P850037 S001

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

DeviceSODIUM CHLORIDE TABLETS, USP
Generic NameAccessories, Soft Lens Products
ApplicantAKORN, INC.
Date Received1986-04-01
Decision Date1986-06-09
PMAP850037
SupplementS001
Product CodeLPN 
Advisory CommitteeOphthalmic
Expedited ReviewNo
Combination Product No
Applicant Address AKORN, INC. 3001 19th St. metairie, LA 70002

Supplemental Filings

Supplement NumberDateSupplement Type
P850037Original Filing
S001 1986-04-01

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