FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TUCKS POLYPAD MATERNITY CARE PAD

K Number: K760924 · Decision Nov 11, 1976
Classifications
1
FEI Numbers
307
Registration Numbers
307
Same Product Code
135
Applicant Total
47
Review Days
14

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
TUCKS POLYPAD MATERNITY CARE PAD
K Number
K760924
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
884.5435
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Parke-Davis Co.
Date Received
October 28, 1976
Decision Date
November 11, 1976
Product Code
HHD
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HHD Pad, Menstrual, Unscented

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HHD), ordered by most recent decision date.

View all

Other Clearances by Parke-Davis Co.

K Number Device Name
K861725 INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT
K862119 DESERET FLO-THRU INJECTATE TEMPERATURE SENSOR
K855120 ATI DISPOSABLE BIOLOGICAL TEST PACK
K860570 ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE
K860290 VIAPIC CENTRAL LINE CATHETER
K852192 DISPOSABLE STEAM BIOLOGICAL TEST PACK
K841967 DESERET THERMODILUTION CARDIAC OUTPUT
K851327 DESERET ARTERIAL CATHETER
K852078 SPECTRUM(TENTATIVE)
K844840 DESERET INTRODUCER SET
Search all 47 clearances from Parke-Davis Co. →