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FDA 510(k)

PROGRAMALITH PROGRAMMER

K-Number: K823242 · 1983-01-08

ApplicantPacesetter Systems
Decision Date1983-01-08
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PROGRAMALITH PROGRAMMER is the device name listed in this FDA 510(k) record. The listed applicant is Pacesetter Systems. It received FDA 510(k) clearance on 1983-01-08 under 510(k) number K823242. The device is classified under product code KNG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROGRAMALITH PROGRAMMER?

PROGRAMALITH PROGRAMMER is a medical device that received FDA 510(k) clearance on 1983-01-08. The listed applicant is Pacesetter Systems. The 510(k) number is K823242.

When did PROGRAMALITH PROGRAMMER receive FDA 510(k) clearance?

PROGRAMALITH PROGRAMMER received FDA 510(k) clearance on 1983-01-08, under 510(k) number K823242.

Who is the listed applicant for PROGRAMALITH PROGRAMMER?

The FDA 510(k) record lists Pacesetter Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROGRAMALITH PROGRAMMER?

The FDA product code for PROGRAMALITH PROGRAMMER is KNG.

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Other records listing Pacesetter Systems as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K910924ENDOCARDIAL LEADS-MOD. TO THE POLYVINYLPYRROLIDONEK902147ENDOCARDIAL SCREW-IN LEAD MODEL 1028TK900512SIEMENS ELEMA MODELS 4020T AND 4021T ADAPTERSK900550FAST-PASS ACE MODELS 1212T/1222T/1216T/1226TK895447ENDOCARDIAL SCREW-IN LEAD MODEL 1020TK891905CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE

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Related Devices (Code: KNG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252669Fetal Doppler U8-25, U9-25Zhongshan Xiaolan Town Senlan Electronic FactoryK242846Doppler FHR Detector (BF-500D+, BF-560)Shenzhen Bestman Instrument Co., Ltd.K233823Ultrasonic Fetal DopplerShenzhen Jamr Technology Co., Ltd.K232893Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC 10E), Pocket Fetal Doppler (CONTEC 10F)Contec Medical Systems Co.,LtdK220245Pocket Fetal Doppler (Models CONTEC10C and CONTEC10CL)Contec Medical Systems Co.,LtdK211940Fetal DopplerShenzhen Taikang Medical Equipment Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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