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FDA 510(k)

DIRECTDRAW SUPERSERUM-MINI

K-Number: K935081 · 1994-01-11

ApplicantInternational Technidyne Corp.
Decision Date1994-01-11
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIRECTDRAW SUPERSERUM-MINI is the device name listed in this FDA 510(k) record. The listed applicant is International Technidyne Corp.. It received FDA 510(k) clearance on 1994-01-11 under 510(k) number K935081. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIRECTDRAW SUPERSERUM-MINI?

DIRECTDRAW SUPERSERUM-MINI is a medical device that received FDA 510(k) clearance on 1994-01-11. The listed applicant is International Technidyne Corp.. The 510(k) number is K935081.

When did DIRECTDRAW SUPERSERUM-MINI receive FDA 510(k) clearance?

DIRECTDRAW SUPERSERUM-MINI received FDA 510(k) clearance on 1994-01-11, under 510(k) number K935081.

Who is the listed applicant for DIRECTDRAW SUPERSERUM-MINI?

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

What is the FDA product code for DIRECTDRAW SUPERSERUM-MINI?

The FDA product code for DIRECTDRAW SUPERSERUM-MINI is JKA.

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Related Devices (Code: JKA)

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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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