DRIP ALERT
Monitor, Electric For Gravity Flow Infusion Systems
DRIP ALERT, INC.
The following data is part of a premarket notification filed by Drip Alert, Inc. with the FDA for Drip Alert.
Pre-market Notification Details
| Device ID | K030136 |
| 510k Number | K030136 |
| Device Name: | DRIP ALERT |
| Classification | Monitor, Electric For Gravity Flow Infusion Systems |
| Applicant | DRIP ALERT, INC. 500 E. BROWARD BLVD. SUITE 1400 Ft. Lauderdale, FL 33394 |
| Contact | Polly D Heseman |
| Correspondent | Polly D Heseman DRIP ALERT, INC. 500 E. BROWARD BLVD. SUITE 1400 Ft. Lauderdale, FL 33394 |
| Product Code | FLN |
| CFR Regulation Number | 880.2420 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-01-14 |
| Decision Date | 2003-04-07 |
| Summary: | summary |
Trademark Results [DRIP ALERT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 DRIP ALERT 78193735 2883401 Dead/Cancelled |
Drip Alert, Inc. 2002-12-12 |
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