FDA product code MPT: Contraception Calculator
MPT is the FDA product code for contraception calculator. It is a Class II device, regulated under 21 CFR 884.5350 and reviewed by the Obstetrics and Gynecology panel. FDA has cleared 1 510(k) submission under MPT. The average 510(k) review took 176 days (median 176).
Classification
| Field | Value |
|---|---|
| Device name | Contraception Calculator |
| Device class | Class II |
| Regulation | 21 CFR 884.5350 |
| Review panel | OB — Obstetrics and Gynecology |
| Medical specialty | Obstetrics/Gynecology |
| Premarket route | 510(k) |
Compare with all 510(k) review times · Search every MPT clearance
Top MPT applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Hector Vides | 1 | 1996-02-29 |
Most recent MPT clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K954183 | Hector Vides | OVULATION CALCULATOR/CONCEPTION CALCULATOR | 1996-02-29 | 176 |
Recalls for MPT devices
openFDA lists no recalls for product code MPT.
Frequently asked questions
What is FDA product code MPT?
MPT is the FDA product code for contraception calculator. It is a Class II device, regulated under 21 CFR 884.5350 and reviewed by the Obstetrics and Gynecology panel.
What device class is MPT?
Class II, regulation 21 CFR 884.5350. Typical premarket route: 510(k).
How long does a 510(k) take for product code MPT?
Across 1 cleared submissions the average was 176 days from receipt to decision (median 176).
Which companies have the most MPT clearances?
Hector Vides (1).
Next steps
- Run an FDA pathway report with predicate devices for product code MPT
- Run a recall and safety report across every MPT manufacturer
- Watch product code MPT for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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