Cleared Traditional

K981760 - PLAYTEX SILK GLIDE ODOR ABSORBING FLUSHABLE CARDBOARD TAMPONS #13598

K981760 is an FDA 510(k) clearance for PLAYTEX SILK GLIDE ODOR ABSORBING FLUSH..., manufactured by Playtime Products, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code HEB cleared through the Traditional 510(k) pathway after a 64-day FDA review.

K981760 · Playtime Products, Inc. · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1998
Decision
64d
Days
Class 2
Risk

K981760 is an FDA 510(k) clearance for the PLAYTEX SILK GLIDE ODOR ABSORBING FLUSHABLE CARDBOARD TAMPONS #13598. Classified as Tampon, Menstrual, Unscented (product code HEB), Class II - Special Controls.

Submitted by Playtime Products, Inc. (Paramus, US). The FDA issued a Cleared decision on July 22, 1998 after a review of 64 days - a notably fast clearance cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.5470 - the FDA obstetrics and gynecology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Playtime Products, Inc. devices

FDA 510(k) Submission Details - K981760

510(k) Number K981760 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 19, 1998
Decision Date July 22, 1998
Days to Decision 64 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
96d faster than avg
Panel avg: 160d · This submission: 64d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HEB Device Classification - Class 2, Special Controls

Product Code HEB Tampon, Menstrual, Unscented
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.5470
Definition An Unscented Menstrual Tampon Is A Plug Made Of Cellulosic Or Synthetic Material That Is Inserted Into The Vagina And Used To Absorb Menstrual Fluid Or Other Vaginal Discharge.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Obstetrics & Gynecology devices follow this clearance model.

Regulatory Peers - HEB Tampon, Menstrual, Unscented

All 136
Devices cleared under the same product code (HEB) and FDA review panel - the closest regulatory comparables to K981760.
ORGANIC ESSENTIALS, ORGANIC COTTON TAMPON
K983478 · Organic Essentials · Nov 1998
VARIOUS TRADE TAMPONS SOLD UNDER PRIVATE LABELS
K983381 · Paragon Trade Brands, Inc. · Oct 1998
VARIOUS TRADE TAMPONS SOLD UNDER PRIVATE LABELS
K981953 · Paragon Trade Brands, Inc. · Aug 1998
PLAYTEX TAMPONS #03498
K980478 · Playtex, Inc. · Apr 1998
O.B. APPLICATOR AND NON-APPLICATOR TAMPONS
K974629 · Personal Products Co. · Feb 1998
O.B. APPLICATOR TAMPONS
K970954 · Personal Products Co. · Jun 1997