TAMPAX PEARL PLASTIC APPLICATOR TAMPONS, SCENTED AND UNSCENTED— 510(k) K081555
Substantially EquivalentProcter & Gamble Co.
FDA 510(k) clearance K081555 for TAMPAX PEARL PLASTIC APPLICATOR TAMPONS, SCENTED AND UNSCENTED, Substantially Equivalent on 2008-06-27. Applicant: Procter & Gamble Co.. Device class: 2.
Clearance details
- Applicant
- Procter & Gamble Co.
- Product code
- Code HIL
- Device class
- Class 2
- Regulation
- 21 CFR 884.5460
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Cincinnati, OH, US
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More clearances from Procter & Gamble Co.
view all- K141018 — ORAL-B TEST DRIVE POWER BRUSH TRIAL PROGRAM KIT, ORAL-B TEST DRIVE POWER TOOTHBRUSH KIT, ORAL-B TEST DRIVE REFILL KIT
- K131543 — TAMPAX(R) L PLASTIC TAMPONS, UNSCENTED
- K091281 — TAMPAX PEARL UNSCENTED TAMPONS, LIGHT, REGULAR, SUPER & SUPER PLUS, TAMPAX PEARL UNSCENTED TAMPONS, ULTRA
- K091964 — CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS
- K062638 — TAMPAX COMPAK PEARL PLASTIC APPLICATOR SCENTED AND UNSCENTED TAMPONS
Recalls naming K081555
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K081555.
Data sourced from openFDA. This site is unofficial and independent of the FDA.