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

3MHZ ANNULAR ARRAY

K Number: K864980 · Decision May 11, 1987
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
71
Applicant Total
46
Review Days
140

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
3MHZ ANNULAR ARRAY
K Number
K864980
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2880
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Philips Ultrasound, Inc.
Date Received
December 22, 1986
Decision Date
May 11, 1987
Product Code
JOP
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
JOP Transducer, Ultrasonic

Similar 510(k) Clearances

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

View all

Other Clearances by Philips Ultrasound, Inc.

K Number Device Name
K212777 Collaboration Live
K203406 Lumify Diagnostic Ultrasound System
K200603 AAA Model
K201665 Collaboration Live
K202216 EPIQ Series Diagnostic Ultrasound Systems
K201053 PercuNav Image Fusion and Interventional Navigation
K201012 EPIQ Diagnostic Ultrasound System Series, Affiniti Diagnostic Ultrasound System Series, CX50 Diagnostic Ultrasound System, Sparq Diagnostic Ultrasound System, Lumify Diagnostic Ultrasound System
K200304 EPIQ Diagnostic Ultrasound System
K182857 EPIQ Diagnostic Ultrasound System, EPIQ 5 Diagnostic Ultrasound System, EPIQ 7 Diagnostic Ultrasound System, Affiniti 30 Diagnostic Ultrasound System, Affiniti 50 Diagnostic Ultrasound System, Affiniti 70 Diagnostic Ultrasound System
K182529 Xperius Ultrasound System
Search all 46 clearances from Philips Ultrasound, Inc. →