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FDA 510(k)

MINIFETON 200

K-Number: K800098 · 1980-02-11

ApplicantKt Medical, Inc.
Decision Date1980-02-11
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MINIFETON 200 is the device name listed in this FDA 510(k) record. The listed applicant is Kt Medical, Inc.. It received FDA 510(k) clearance on 1980-02-11 under 510(k) number K800098. 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 MINIFETON 200?

MINIFETON 200 is a medical device that received FDA 510(k) clearance on 1980-02-11. The listed applicant is Kt Medical, Inc.. The 510(k) number is K800098.

When did MINIFETON 200 receive FDA 510(k) clearance?

MINIFETON 200 received FDA 510(k) clearance on 1980-02-11, under 510(k) number K800098.

Who is the listed applicant for MINIFETON 200?

The FDA 510(k) record lists Kt Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINIFETON 200?

The FDA product code for MINIFETON 200 is KNG.

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Other records listing Kt Medical, Inc. 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.

K800653SINVISION LINEAR ARRAY REAL TIMEK800652MODEL E03 ECHO-OPTHALMOSCOPEK8001014200 ME ECHOENCEPHALOGRAPHK800092COMBISON COMPUTERK800099INTRACULA IIK8001007200 MA ECHO-OPHTHALMOSCOPE

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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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