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FDA 510(k)

KELLER CARDIAC MONITOR MEDIL KMS870

K-Number: K914576 · 1991-12-30

ApplicantKeller Medical Specialties Products, Inc.
Decision Date1991-12-30
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KELLER CARDIAC MONITOR MEDIL KMS870 is the device name listed in this FDA 510(k) record. The listed applicant is Keller Medical Specialties Products, Inc.. It received FDA 510(k) clearance on 1991-12-30 under 510(k) number K914576. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KELLER CARDIAC MONITOR MEDIL KMS870?

KELLER CARDIAC MONITOR MEDIL KMS870 is a medical device that received FDA 510(k) clearance on 1991-12-30. The listed applicant is Keller Medical Specialties Products, Inc.. The 510(k) number is K914576.

When did KELLER CARDIAC MONITOR MEDIL KMS870 receive FDA 510(k) clearance?

KELLER CARDIAC MONITOR MEDIL KMS870 received FDA 510(k) clearance on 1991-12-30, under 510(k) number K914576.

Who is the listed applicant for KELLER CARDIAC MONITOR MEDIL KMS870?

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

What is the FDA product code for KELLER CARDIAC MONITOR MEDIL KMS870?

The FDA product code for KELLER CARDIAC MONITOR MEDIL KMS870 is DRT.

Related Clinical Trials

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.

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Other records listing Keller Medical Specialties Products, 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.

K990648KELLER VITAL SIGNS MONITOR, KMS 890+K982331KELLER PULSE OXIMETER, MODEL 850+K910262KELLER VITAL SIGNS MONITOR - KMS-890K903437DISPOS ACCESS EXTERNAL CARDIAC PACEMAKERK895987KELLER PULSE OXIMETER - KMS 850

Related Devices (Code: DRT)

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.

K254058DistaSense(TM) (v1)Life Detection TechnologiesK261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.

Official Source

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

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