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FDA 510(k)

INFORMER PLUS

K-Number: K943481 · 1994-11-02

ApplicantMicro-Tech Medical, Inc.
Decision Date1994-11-02
Product CodeKMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFORMER PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Tech Medical, Inc.. It received FDA 510(k) clearance on 1994-11-02 under 510(k) number K943481. The device is classified under product code KMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFORMER PLUS?

INFORMER PLUS is a medical device that received FDA 510(k) clearance on 1994-11-02. The listed applicant is Micro-Tech Medical, Inc.. The 510(k) number is K943481.

When did INFORMER PLUS receive FDA 510(k) clearance?

INFORMER PLUS received FDA 510(k) clearance on 1994-11-02, under 510(k) number K943481.

Who is the listed applicant for INFORMER PLUS?

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

What is the FDA product code for INFORMER PLUS?

The FDA product code for INFORMER PLUS is KMI.

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Related Devices (Code: KMI)

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.

K131585INTEL-GE CARE INNOVATIONS QUIETCAREIntel-Ge Care Innovations, LLCK130752DYNASENSE SYSTEMCentauri Medical, Inc.K101109VIVATRAKWireless Medcare, LLCK090138MOBILECARE MONITOR, MODEL 2100Aframe Digital, Inc.K942770ULTIMAT-SENSOR FOR BED OCCUPANCY MONITORUltimate Development Corp.K933552PM-PAGERHill Engineering

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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