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FDA 510(k)

GRAHAM-FIELD ULTRASOUND LOTION

K-Number: K944596 · 1995-06-07

ApplicantChester Labs, Inc.
Decision Date1995-06-07
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GRAHAM-FIELD ULTRASOUND LOTION is the device name listed in this FDA 510(k) record. The listed applicant is Chester Labs, Inc.. It received FDA 510(k) clearance on 1995-06-07 under 510(k) number K944596. 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 GRAHAM-FIELD ULTRASOUND LOTION?

GRAHAM-FIELD ULTRASOUND LOTION is a medical device that received FDA 510(k) clearance on 1995-06-07. The listed applicant is Chester Labs, Inc.. The 510(k) number is K944596.

When did GRAHAM-FIELD ULTRASOUND LOTION receive FDA 510(k) clearance?

GRAHAM-FIELD ULTRASOUND LOTION received FDA 510(k) clearance on 1995-06-07, under 510(k) number K944596.

Who is the listed applicant for GRAHAM-FIELD ULTRASOUND LOTION?

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

What is the FDA product code for GRAHAM-FIELD ULTRASOUND LOTION?

The FDA product code for GRAHAM-FIELD ULTRASOUND LOTION is IMI.

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Other records listing Chester Labs, 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.

K041060E-Z LUBRICATING JELLYK001705STATSIGN ELECTRODE CONDUCTIVITY GEL, GRAHAM-FIELD ELECTRODE CONDUCTIVITY GEL, MODELS 004008, 48-4000 2GF, 48-4000GFK001593MODIFICATION TO STATSIGN SALINE ELECTROLYTE GEL, GRAHAM-FIELD SALINE ELECTROLYTE GELK944598GRAHAM-FIELD ELECTRODE CONDUCTIVITY GELK944599GRAHAM-FIELD CONDUCTIVE ECG SPRAYK944600GRAHAM-FIELD SALINE ELECTROLYTE GEL

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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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