The following data is part of a premarket notification filed by Ferguson Medical with the FDA for Dp 100.
Device ID | K911192 |
510k Number | K911192 |
Device Name: | DP 100 |
Classification | Nebulizer (direct Patient Interface) |
Applicant | FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619 |
Contact | Frank Ferguson |
Correspondent | Frank Ferguson FERGUSON MEDICAL 3407 BAY AVE. Chico, CA 95973 -8619 |
Product Code | CAF |
CFR Regulation Number | 868.5630 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-03-18 |
Decision Date | 1991-12-11 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DP 100 74051083 1634722 Dead/Cancelled |
Analogic Corporation 1990-04-20 |