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FDA 510(k)

MULTIDRAW SYSTEM

K-Number: K922858 · 1992-11-16

ApplicantCambridge Multi-Draw, Inc.
Decision Date1992-11-16
Product CodeGIM
Advisory CommitteeCH
DecisionUnknown

Device Summary

MULTIDRAW SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Multi-Draw, Inc.. It received FDA 510(k) clearance on 1992-11-16 under 510(k) number K922858. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MULTIDRAW SYSTEM?

MULTIDRAW SYSTEM is a medical device that received FDA 510(k) clearance on 1992-11-16. The listed applicant is Cambridge Multi-Draw, Inc.. The 510(k) number is K922858.

When did MULTIDRAW SYSTEM receive FDA 510(k) clearance?

MULTIDRAW SYSTEM received FDA 510(k) clearance on 1992-11-16, under 510(k) number K922858.

Who is the listed applicant for MULTIDRAW SYSTEM?

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

What is the FDA product code for MULTIDRAW SYSTEM?

The FDA product code for MULTIDRAW SYSTEM is GIM.

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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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