The following data is part of a premarket notification filed by Monaghan Medical Corp. with the FDA for Modification To Trupeak Peak Flow Meter.
| Device ID | K031514 |
| 510k Number | K031514 |
| Device Name: | MODIFICATION TO TRUPEAK PEAK FLOW METER |
| Classification | Meter, Peak Flow, Spirometry |
| Applicant | MONAGHAN MEDICAL CORP. 5 LATOUR AVE., SUITE 1600 P.O. BOX 2805 Plattsburgh, NY 12901 |
| Contact | James A Cochie |
| Correspondent | James A Cochie MONAGHAN MEDICAL CORP. 5 LATOUR AVE., SUITE 1600 P.O. BOX 2805 Plattsburgh, NY 12901 |
| Product Code | BZH |
| CFR Regulation Number | 868.1860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-05-14 |
| Decision Date | 2003-05-23 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50604351965107 | K031514 | 000 |
| 00604351965010 | K031514 | 000 |
| 50604351915102 | K031514 | 000 |
| 50604351915010 | K031514 | 000 |