Cleared Traditional

PADS, MINI, MAXI DEODORANT (K782111) - FDA 510(k) Clearance

Class II Obstetrics & Gynecology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K782111 · Intl. Playtex, Inc. · Obstetrics & Gynecology device
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Jan 1979
Decision
21d
Days
Class 2
Risk

K782111 is an FDA 510(k) clearance for the PADS, MINI, MAXI DEODORANT. Classified as Pad, Menstrual, Scented, Scented-deodorized (product code HHL), Class II - Special Controls.

Submitted by Intl. Playtex, Inc. (Walker, US). The FDA issued a Cleared decision on January 8, 1979 after a review of 21 days - a notably fast clearance cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.5425 - 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 Intl. Playtex, Inc. devices

Submission Details

510(k) Number K782111 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 18, 1978
Decision Date January 08, 1979
Days to Decision 21 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
139d faster than avg
Panel avg: 160d · This submission: 21d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HHL Pad, Menstrual, Scented, Scented-deodorized
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.5425
Definition Scented Or Scented-deodorized Menstrual Pads Used To Absorb Menstrual Or Other Vaginal Discharge, Including Those Intended As Intralabial Pads Or Reusable Menstrual Pads. These Are Made With Materials That Do Not Meet The Requirements For Class 1 Per 21 Cfr 884.5425(b).
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 - HHL Pad, Menstrual, Scented, Scented-deodorized

All 56
Devices cleared under the same product code (HHL) and FDA review panel - the closest regulatory comparables to K782111.
SURE & NATURAL DEODORANT MAXI-SHIELD
K843155 · Johnson & Johnson Professionals, Inc. · Aug 1984
STAYFREE* DEODORANT MAXI-PADS
K834302 · Johnson & Johnson Professionals, Inc. · Jan 1984
CAREFREE * PANTY SHIELDS-REG/DEOR
K832382 · Johnson & Johnson Professionals, Inc. · Aug 1983
PETITES BETWEEN-PERIOD PROTECTORS
K771547 · 3M Company · Sep 1977