THE AMCON WAY PLUS

FDA Premarket Approval P800069 S002

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

DeviceTHE AMCON WAY PLUS
Generic NameAccessories, Soft Lens Products
ApplicantAMCON, INC.
Date Received1982-05-12
Decision Date1982-10-05
Notice Date1983-02-22
PMAP800069
SupplementS002
Product CodeLPN 
Advisory CommitteeOphthalmic
Expedited ReviewNo
Combination Product No
Applicant Address AMCON, INC. 1102 Main St. p.o. Box 176 grandview, MO 64030

Supplemental Filings

Supplement NumberDateSupplement Type
P800069Original Filing
S009 1987-11-24 Special (immediate Track)
S008 1986-06-18 Normal 180 Day Track
S007 1985-05-24
S006 1985-04-16
S005
S004 1982-05-12
S003 1982-05-12
S002 1982-05-12
S001 1982-01-15

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