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.
Device | SODIUM CHLORIDE TABLETS, USP |
Generic Name | Accessories, Soft Lens Products |
Applicant | AKORN, INC. |
Date Received | 1986-04-01 |
Decision Date | 1986-06-09 |
PMA | P850037 |
Supplement | S001 |
Product Code | LPN |
Advisory Committee | Ophthalmic |
Expedited Review | No |
Combination Product | No |
Applicant Address | AKORN, INC. 3001 19th St. metairie, LA 70002 |
Supplement Number | Date | Supplement Type |
---|---|---|
P850037 | Original Filing | |
S001 | 1986-04-01 |