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FDA 510(k)

MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI.

K-Number: K871869 · 1987-08-11

ApplicantLife-Tech Intl., Inc.
Decision Date1987-08-11
Product CodeEGJ
Advisory CommitteePM
DecisionUnknown

Device Summary

MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI. 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 1987-08-11 under 510(k) number K871869. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI.?

MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI. is a medical device that received FDA 510(k) clearance on 1987-08-11. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K871869.

When did MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI. receive FDA 510(k) clearance?

MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI. received FDA 510(k) clearance on 1987-08-11, under 510(k) number K871869.

Who is the listed applicant for MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI.?

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 MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI.?

The FDA product code for MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI. is EGJ.

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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.

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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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