RELY TAMPON
FDA 510(k) clearance K761184 · decided 1976-12-17
Clearance details
- K-number
- K761184
- Device name
- RELY TAMPON
- Applicant
- Procter & Gamble Mfg. Co.
- Decision
- Substantially Equivalent
- Date received
- 1976-12-03
- Decision date
- 1976-12-17
- Days to decision
- 14 days
- Clearance type
- Traditional
- Product code
- HIL
- Device class
- 2
- Regulation number
- 884.5460
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.