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

TRINITY SLEEVES, HUNTLEIGH PUMP COMPATIBLE(T.B.D.)

K Number: K970014 · Decision Aug 6, 1997
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
349
Applicant Total
6
Review Days
216

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
TRINITY SLEEVES, HUNTLEIGH PUMP COMPATIBLE(T.B.D.)
K Number
K970014
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Delphi Consulting Group
Date Received
January 2, 1997
Decision Date
August 6, 1997
Product Code
JOW
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
JOW Sleeve, Limb, Compressible

Similar 510(k) Clearances

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

View all

Other Clearances by Delphi Consulting Group

K Number Device Name
K983680 TRINITY II SINGLE CHAMBER DVT PUMP
K963957 TRINITY DVT SYSTEM
K961937 SIMULSCOPE AUSCULTATION AND SIMULSCOPE BEDSIDE AUSCULTATION SYSTEM
K961301 E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120
K954489 TRINITY SLEEVE(S)