FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SCHULMAN DOUBLE UMBILICAL CORD CLAMP NO. 1000

K Number: K863645 · Decision Sep 25, 1986
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
35
Applicant Total
5
Review Days
7

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
SCHULMAN DOUBLE UMBILICAL CORD CLAMP NO. 1000
K Number
K863645
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
United Medical Systems, Inc.
Date Received
September 18, 1986
Decision Date
September 25, 1986
Product Code
HFW
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
HFW Clamp, Umbilical

Similar 510(k) Clearances

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

View all

Other Clearances by United Medical Systems, Inc.

K Number Device Name
K072538 PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPTER
K032958 PIEZOLITH 3000 LITHOTRIPTER, MODEL 3000
K894949 SQA
K893003 TOCOLYTIC SITE CARE SUP KIT #1001/100A/CARRY CASE