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FDA 510(k)

IONTOPHORESIS SYSTEM MODULE, DM 500

K-Number: K770717 · 1977-08-15

ApplicantSorensen Research
Decision Date1977-08-15
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

IONTOPHORESIS SYSTEM MODULE, DM 500 is the device name listed in this FDA 510(k) record. The listed applicant is Sorensen Research. It received FDA 510(k) clearance on 1977-08-15 under 510(k) number K770717. 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 IONTOPHORESIS SYSTEM MODULE, DM 500?

IONTOPHORESIS SYSTEM MODULE, DM 500 is a medical device that received FDA 510(k) clearance on 1977-08-15. The listed applicant is Sorensen Research. The 510(k) number is K770717.

When did IONTOPHORESIS SYSTEM MODULE, DM 500 receive FDA 510(k) clearance?

IONTOPHORESIS SYSTEM MODULE, DM 500 received FDA 510(k) clearance on 1977-08-15, under 510(k) number K770717.

Who is the listed applicant for IONTOPHORESIS SYSTEM MODULE, DM 500?

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

What is the FDA product code for IONTOPHORESIS SYSTEM MODULE, DM 500?

The FDA product code for IONTOPHORESIS SYSTEM MODULE, DM 500 is EGJ.

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Other records listing Sorensen Research as applicant

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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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