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FDA 510(k)

MEDITHERM

K-Number: K894152 · 1990-06-11

ApplicantMedical Equipment Designs, Inc.
Decision Date1990-06-11
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDITHERM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Equipment Designs, Inc.. It received FDA 510(k) clearance on 1990-06-11 under 510(k) number K894152. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDITHERM?

MEDITHERM is a medical device that received FDA 510(k) clearance on 1990-06-11. The listed applicant is Medical Equipment Designs, Inc.. The 510(k) number is K894152.

When did MEDITHERM receive FDA 510(k) clearance?

MEDITHERM received FDA 510(k) clearance on 1990-06-11, under 510(k) number K894152.

Who is the listed applicant for MEDITHERM?

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

What is the FDA product code for MEDITHERM?

The FDA product code for MEDITHERM is IMI.

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Other records listing Medical Equipment Designs, 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.

K911308CARDIOTRACE-I TRANSTELEPHONIC ECG RECEIV CONSOLEK895375MULTISPIROK851277MICROSPIRO-SDSK840929FRC 85 SERIES SPIROMETERK840908CHESTAC-25F SPIROMETERK821082TRIAL LENS SET

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Related Devices (Code: IMI)

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.

K240788Ultrasound StimulatorJkh Health Co., Ltd.K230472Sonopuls 190Enraf-Nonius, B.V.K222098ManaSport+Manamed, Inc.K210284ManaSportManamed, Inc.K202788Sonomed IV, Sonomed VCarci Industria E Comercio DE Aparelhos Cirurgicos E OrtoK160378BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS)Brh Medical , 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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