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FDA 510(k)

LOGIKAL LONTOPHORESIS UNIT -ANESTHESIA INOTOPHORES

K-Number: K850508 · 1985-05-15

ApplicantKal Life Systems
Decision Date1985-05-15
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LOGIKAL LONTOPHORESIS UNIT -ANESTHESIA INOTOPHORES is the device name listed in this FDA 510(k) record. The listed applicant is Kal Life Systems. It received FDA 510(k) clearance on 1985-05-15 under 510(k) number K850508. 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 LOGIKAL LONTOPHORESIS UNIT -ANESTHESIA INOTOPHORES?

LOGIKAL LONTOPHORESIS UNIT -ANESTHESIA INOTOPHORES is a medical device that received FDA 510(k) clearance on 1985-05-15. The listed applicant is Kal Life Systems. The 510(k) number is K850508.

When did LOGIKAL LONTOPHORESIS UNIT -ANESTHESIA INOTOPHORES receive FDA 510(k) clearance?

LOGIKAL LONTOPHORESIS UNIT -ANESTHESIA INOTOPHORES received FDA 510(k) clearance on 1985-05-15, under 510(k) number K850508.

Who is the listed applicant for LOGIKAL LONTOPHORESIS UNIT -ANESTHESIA INOTOPHORES?

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

What is the FDA product code for LOGIKAL LONTOPHORESIS UNIT -ANESTHESIA INOTOPHORES?

The FDA product code for LOGIKAL LONTOPHORESIS UNIT -ANESTHESIA INOTOPHORES 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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