Atlas FDA

ALWAYS DUETS

FDA 510(k) clearance K012629 · decided 2001-10-05

Clearance details

K-number
K012629
Device name
ALWAYS DUETS
Applicant
Procter & Gamble Co.
Decision
Substantially Equivalent
Date received
2001-08-13
Decision date
2001-10-05
Days to decision
53 days
Clearance type
Traditional
Product code
HHD
Device class
1
Regulation number
884.5435
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Cincinnati, OH, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
ALWAYS MENSTRUAL PADS (K071827)Procter & Gamble, Inc.2007-09-20
ENVIVE MINIFORMS (K003843)Procter & Gamble Co.2001-02-08
UNSCENTED INTERLABIAL MENSTRUAL PAD (K993870)Procter & Gamble Co.2000-01-18
GLADRAGS COTTON MENSTRUAL PAD (K980395)Keepers!, Inc.1998-04-16
FLUSHIES FLUSHABLE/BIODEGRADABLE MENSTRUAL PADS/NAPKINS (ULTRA THINS) (K953470)Mediquip, Inc.1995-11-21
UNSCENTED ULTRATHIN MAXI PAD (K953668)Paragon Trade Brands, Inc.1995-11-01
UNSCENTED MENSTRUAL PAD (K953633)Tendasoft, Inc.1995-11-01
UNSCENTED CURVED ULTRATHIN MAXI PADS (K953667)Paragon Trade Brands, Inc.1995-11-01
UNSCENTED MENSTRAL PAD (K953553)Paragon Trade Brands, Inc.1995-10-27
UNSCENTED MENSTRUAL PAD (K953517)Paragon Trade Brands, Inc.1995-10-26
UNSCENTED CURVED MAXI PAD (K953700)Paragon Trade Brands, Inc.1995-09-27
UNSCENTED MENSTRAL PAD WITH WINGS (K953666)Paragon Trade Brands, Inc.1995-09-27

Recalls involving this device

No recalls on record reference this clearance.