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FDA 510(k)

MS-III MINISTIM

K-Number: K913184 · 1991-10-07

ApplicantLife-Tech Intl., Inc.
Decision Date1991-10-07
Product CodeBXN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MS-III MINISTIM is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech Intl., Inc.. It received FDA 510(k) clearance on 1991-10-07 under 510(k) number K913184. The device is classified under product code BXN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MS-III MINISTIM?

MS-III MINISTIM is a medical device that received FDA 510(k) clearance on 1991-10-07. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K913184.

When did MS-III MINISTIM receive FDA 510(k) clearance?

MS-III MINISTIM received FDA 510(k) clearance on 1991-10-07, under 510(k) number K913184.

Who is the listed applicant for MS-III MINISTIM?

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

What is the FDA product code for MS-III MINISTIM?

The FDA product code for MS-III MINISTIM is BXN.

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Other records listing Life-Tech Intl., 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.

K001129PROLONG, MODELS PL50, PL100, PL150K954505EZ STIMK955031MAXISTIMK954315PVC ABDOMINAL/RECTAL PRESSURE CATHETERK954341URODYNAMICS TUBING AND INFUSION SETSK953451UROPUMP TUBE & DAMPING CHAMGER

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Related Devices (Code: BXN)

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.

K213049STIMPOD NMS450 Nerve StimulatorXavant Technology (Pty), Ltd.K162086MultiStim ECOPAJUNK GmbH MedizintechnologieK153045SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve StimulatorEasy Med Instrument Co., Ltd.K121743EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTINSunmed, LLCK111985MYOGUIDE SYSTEM MODEL 8008Intronix Technologies Corp.K110118STIMTRODE SINGLE USE NERVE STIMULATORXavant Technology (Pty), 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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