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FDA 510(k)

ELECTROAPPLICATOR MODEL C-1

K-Number: K790205 · 1979-03-19

ApplicantMcg, Inc.
Decision Date1979-03-19
Product CodeKTB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTROAPPLICATOR MODEL C-1 is the device name listed in this FDA 510(k) record. The listed applicant is Mcg, Inc.. It received FDA 510(k) clearance on 1979-03-19 under 510(k) number K790205. 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 ELECTROAPPLICATOR MODEL C-1?

ELECTROAPPLICATOR MODEL C-1 is a medical device that received FDA 510(k) clearance on 1979-03-19. The listed applicant is Mcg, Inc.. The 510(k) number is K790205.

When did ELECTROAPPLICATOR MODEL C-1 receive FDA 510(k) clearance?

ELECTROAPPLICATOR MODEL C-1 received FDA 510(k) clearance on 1979-03-19, under 510(k) number K790205.

Who is the listed applicant for ELECTROAPPLICATOR MODEL C-1?

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

What is the FDA product code for ELECTROAPPLICATOR MODEL C-1?

The FDA product code for ELECTROAPPLICATOR MODEL C-1 is KTB.

Related Clinical Trials

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.

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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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