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

PROGRAMALITH PROGRAMMER

K Number: K823242 · Decision Jan 8, 1983
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
59
Applicant Total
96
Review Days
68

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Basic Information

Device Name
PROGRAMALITH PROGRAMMER
K Number
K823242
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.2660
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Pacesetter Systems
Date Received
November 1, 1982
Decision Date
January 8, 1983
Product Code
KNG
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
KNG Monitor, Ultrasonic, Fetal

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K Number Device Name
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K900512 SIEMENS ELEMA MODELS 4020T AND 4021T ADAPTERS
K900550 FAST-PASS ACE MODELS 1212T/1222T/1216T/1226T
K895447 ENDOCARDIAL SCREW-IN LEAD MODEL 1020T
K891905 CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE
K885267 VS-1 MODEL NUMBER 251K PULSE GENERATOR
K890547 SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS
K884733 AFP MODEL 262T PULSE GENERATOR
K883087 PROLOG MP 658M PULSE GENERATOR
Search all 96 clearances from Pacesetter Systems →