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FDA 510(k)

MEDSIM 300 PATIENT SIMULATOR

K-Number: K935817 · 1994-01-18

ApplicantDynatech/Nevada, Inc.
Decision Date1994-01-18
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDSIM 300 PATIENT SIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech/Nevada, Inc.. It received FDA 510(k) clearance on 1994-01-18 under 510(k) number K935817. 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 MEDSIM 300 PATIENT SIMULATOR?

MEDSIM 300 PATIENT SIMULATOR is a medical device that received FDA 510(k) clearance on 1994-01-18. The listed applicant is Dynatech/Nevada, Inc.. The 510(k) number is K935817.

When did MEDSIM 300 PATIENT SIMULATOR receive FDA 510(k) clearance?

MEDSIM 300 PATIENT SIMULATOR received FDA 510(k) clearance on 1994-01-18, under 510(k) number K935817.

Who is the listed applicant for MEDSIM 300 PATIENT SIMULATOR?

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

What is the FDA product code for MEDSIM 300 PATIENT SIMULATOR?

The FDA product code for MEDSIM 300 PATIENT SIMULATOR 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 Dynatech/Nevada, 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.

K942546CUFFLINK NON-INVASIVE BLOOD PRESSURE ANALYZERK934254IMPULSE 3000 DEFIBRILLATOR ANALYZERK897074MODEL 215M PATIENT SIMULATORK897029MODEL ECG100 SIMULATORK897096MODEL 404A I.V. INFUSION PUMP ANALYZER

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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