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FDA 510(k)

MODEL 6110 IONTOPHORETIC APPLICATOR

K-Number: K863166 · 1987-03-04

ApplicantLife-Tech Intl., Inc.
Decision Date1987-03-04
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL 6110 IONTOPHORETIC APPLICATOR 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 1987-03-04 under 510(k) number K863166. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 6110 IONTOPHORETIC APPLICATOR?

MODEL 6110 IONTOPHORETIC APPLICATOR is a medical device that received FDA 510(k) clearance on 1987-03-04. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K863166.

When did MODEL 6110 IONTOPHORETIC APPLICATOR receive FDA 510(k) clearance?

MODEL 6110 IONTOPHORETIC APPLICATOR received FDA 510(k) clearance on 1987-03-04, under 510(k) number K863166.

Who is the listed applicant for MODEL 6110 IONTOPHORETIC APPLICATOR?

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 MODEL 6110 IONTOPHORETIC APPLICATOR?

The FDA product code for MODEL 6110 IONTOPHORETIC APPLICATOR is EGJ.

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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, PL150K955031MAXISTIMK954505EZ STIMK954315PVC ABDOMINAL/RECTAL PRESSURE CATHETERK954341URODYNAMICS TUBING AND INFUSION SETSK953451UROPUMP TUBE & DAMPING CHAMGER

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Related Devices (Code: EGJ)

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.

K242041STOPWET iontophoresis apparatus (SW01)Taiwan Medical Electronics Co., Ltd.K241267Hidroxa SE30Hidroxa Medical ABK232020Iontophoresis ElectrodesTop-Rank Health Care Co., Ltd.K192749DermadryDermadry Laboratories, Inc.K191436SaalioSaalmann Medical GmbH & Co. KGK170835Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITEHightech Development

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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