Atlas FDA

NIPLETTE

FDA 510(k) clearance K952035 · decided 1995-07-28

Clearance details

K-number
K952035
Device name
NIPLETTE
Applicant
Avent America, Inc.
Decision
Substantially Equivalent
Date received
1995-05-01
Decision date
1995-07-28
Days to decision
88 days
Clearance type
Traditional
Product code
HGY
Device class
1
Regulation number
884.5150
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Addison, IL, 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
HANDHELD MANUAL BREAST PUMP (AVENT MANUAL BREAST PUMP) (K101538)Philips Electronics UK Limited2010-11-05
EASY COMFORT DELUXE MANUAL BREAST PUMP, MODEL 1187 (K032845)The First Years, Inc.2004-04-05
EVENFLO COMFORT EASE MANUAL BREAST PUMP KIT (K013226)Evenflo Company, Inc.2001-12-20
AMEDA HYGIENIKIT (K011519)Hollister, Inc.2001-08-15
WHITE RIVER MINI MANUAL BREAST PUMP (K971231)White River Concepts1997-05-19
EVERT-IT (K962828)Genesis Industries, Inc.1997-02-10
MEDELA'S FOOT PUMP (K952034)Medela, Inc.1995-09-12
WHITE RIVER MANUAL BREAST PUMP (K925738)White River (Tm)1994-05-04
MOTHERS TOUCH ONE HAND BREAST PUMP (K912355)Hollister, Inc.1993-12-10
GERBER PRECIOUS CARE ELECTRIC BREAST PUMP (K902552)Gerber Products Co.1990-09-26
CRYSTAL MANUAL BREAST PUMP (K850242)Crystal Medical Products, Inc.1985-02-25
SUPPLEMENTAL FEEDING SYSTEM (K844297)Medela, Inc.1985-02-25

Recalls involving this device

No recalls on record reference this clearance.