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

PFIZER/AS&E 0450 LOCALIZER

K Number: K800501 · Decision Apr 10, 1980
Classifications
1
FEI Numbers
36
Registration Numbers
37
Same Product Code
22
Applicant Total
12
Review Days
37

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
PFIZER/AS&E 0450 LOCALIZER
K Number
K800501
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.4580
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Pfizer Medical Systems, Inc.
Date Received
March 4, 1980
Decision Date
April 10, 1980
Product Code
JDX
Advisory Committee
Orthopedic
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
JDX Instrument, Surgical, Sonic And Accessory/Attachment

Similar 510(k) Clearances

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

View all

Other Clearances by Pfizer Medical Systems, Inc.

K Number Device Name
K803032 PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL.
K802529 PFIZONIC 100 ULTRASOUND SCANNER
K802528 PFIZONIC 150 ULTRASOUND SCANNER
K802532 PFIZONIC 300 ULTRASOUND SCANNER
K802531 PFIZONIC 200 ULTRASOUND SCANNER
K802530 PFIZONIC 250 ULTRASOUND SCANNER
K801446 PFIZER PZ-CT SCANNER
K781752 SCANNER, CT 0450
K780278 RADIATION THERAPY TREAT. PLAN. SYS.
K772289 SCANNER, CT, 0400
Search all 12 clearances from Pfizer Medical Systems, Inc. →