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FDA 510(k)

MICROVIT MT-100

K-Number: K973735 · 1998-08-25

ApplicantSchiller America, Inc.
Decision Date1998-08-25
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICROVIT MT-100 is the device name listed in this FDA 510(k) record. The listed applicant is Schiller America, Inc.. It received FDA 510(k) clearance on 1998-08-25 under 510(k) number K973735. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROVIT MT-100?

MICROVIT MT-100 is a medical device that received FDA 510(k) clearance on 1998-08-25. The listed applicant is Schiller America, Inc.. The 510(k) number is K973735.

When did MICROVIT MT-100 receive FDA 510(k) clearance?

MICROVIT MT-100 received FDA 510(k) clearance on 1998-08-25, under 510(k) number K973735.

Who is the listed applicant for MICROVIT MT-100?

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

What is the FDA product code for MICROVIT MT-100?

The FDA product code for MICROVIT MT-100 is DSH.

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Other records listing Schiller America, 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.

K973751MT-200K970879CARDIOVIT CS-200K953396CARDIOVIT AT-1C, AT-2CK954066MINISCOPE MS-3K941462CARDIOVIT AT-5CK946205CARDIOVIT AT-1, P-80

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Related Devices (Code: DSH)

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.

K260157LifeLens Physiological MonitorLifeLens Technologies, Inc.K252389Rhythm Master ECG Patch (HM-15BB-AX, HM-15BW-AX, HM-15BW-DX)Smwmed, Inc.K253293VitaloJAK Clinic (Model 7100)Vitalograph , Ltd.K243650Zio® monitor (DFG0001)iRhythm Technologies, Inc.K243603AeviceMDAevice Health Pte. , Ltd.K242583AT-Patch (ATP-C130/ATP-C70)Atsens 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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