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FDA 510(k)

IONOTPHORETIC APPLICATOR

K-Number: K781700 · 1978-11-03

ApplicantMcghan Medical Corp.
Decision Date1978-11-03
Product CodeKTB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

IONOTPHORETIC APPLICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Mcghan Medical Corp.. It received FDA 510(k) clearance on 1978-11-03 under 510(k) number K781700. The device is classified under product code KTB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IONOTPHORETIC APPLICATOR?

IONOTPHORETIC APPLICATOR is a medical device that received FDA 510(k) clearance on 1978-11-03. The listed applicant is Mcghan Medical Corp.. The 510(k) number is K781700.

When did IONOTPHORETIC APPLICATOR receive FDA 510(k) clearance?

IONOTPHORETIC APPLICATOR received FDA 510(k) clearance on 1978-11-03, under 510(k) number K781700.

Who is the listed applicant for IONOTPHORETIC APPLICATOR?

The FDA 510(k) record lists Mcghan Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IONOTPHORETIC APPLICATOR?

The FDA product code for IONOTPHORETIC APPLICATOR is KTB.

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Other records listing Mcghan Medical Corp. 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.

K873475MICRO-TORQUE HAND ENGINE & ACCESS. DERMABRA. BURSK873476MINI-MOTOR HAND ENGINE & ACCESS. DERMABRASION BURSK870754MCGHAN TISSUE EXPANDER FILL SYSTEMK864185MCGHAN LONGTERM MAMMARY EXPANDER, RTV DESIGNK864184MCGHAN LONGTERM MAMMARY EXPANDER/GEL-SALINE DESIGNK862203MCGHAN MAGNA-SITE(TM) TISSUE EXPANDER

View all 14 devices →

Related Devices (Code: KTB)

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.

K180627Macroduct Advanced Model 3710Elitechgroup, Inc.K033192RH-950Iomed, Inc.K031551NORTHSTAR LIDOCAINE IONTOPHORETIC CONTROLLER (NORTHSTAR CONTROLLER-D)Vyteris, Inc.K031115RH-900Iomed, Inc.K010031NANODUCT NEONATAL SWEAT ANALYSIS SYSTEMWescor, Inc.K001522TRANSQ3Iomed, Inc.

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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