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FDA 510(k)

MEDISTOR II

K-Number: K790579 · 1979-04-04

ApplicantCybermedic, Inc.
Decision Date1979-04-04
Product CodeBTY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDISTOR II is the device name listed in this FDA 510(k) record. The listed applicant is Cybermedic, Inc.. It received FDA 510(k) clearance on 1979-04-04 under 510(k) number K790579. The device is classified under product code BTY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDISTOR II?

MEDISTOR II is a medical device that received FDA 510(k) clearance on 1979-04-04. The listed applicant is Cybermedic, Inc.. The 510(k) number is K790579.

When did MEDISTOR II receive FDA 510(k) clearance?

MEDISTOR II received FDA 510(k) clearance on 1979-04-04, under 510(k) number K790579.

Who is the listed applicant for MEDISTOR II?

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

What is the FDA product code for MEDISTOR II?

The FDA product code for MEDISTOR II is BTY.

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Other records listing Cybermedic, 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.

K941813VENSHIELDK914205PFF-1K903959NEONATAL METASCOPEK884910MODEL 1010, CY-METK861418SPINNAKERK851197CYBERMEDIC CM-810 BODY PLETHYSMOGRAPH

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Related Devices (Code: BTY)

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.

K260242CPETWise PlatformMedibyt , Ltd.K242809Ascent Cardiorespiratory Diagnostic SoftwareMedical Graphics CorporationK223629SpiroSphere, SpiroSphereECG, CardioSphereEresearchtechnology GmbHK231561Pulmonary Function Tester, Model: A9Guangzhou Homesun Medical Technology Co., Ltd.K222982Virtus Metabolic MonitorVirtus Technology ApsK221030Model 9100 PFT/DICOVitalograph Ireland, 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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