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FDA 510(k)

CEFAR DUAL

K-Number: K883236 · 1988-11-16

ApplicantCefar Medical Products, Inc.
Decision Date1988-11-16
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CEFAR DUAL is the device name listed in this FDA 510(k) record. The listed applicant is Cefar Medical Products, Inc.. It received FDA 510(k) clearance on 1988-11-16 under 510(k) number K883236. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEFAR DUAL?

CEFAR DUAL is a medical device that received FDA 510(k) clearance on 1988-11-16. The listed applicant is Cefar Medical Products, Inc.. The 510(k) number is K883236.

When did CEFAR DUAL receive FDA 510(k) clearance?

CEFAR DUAL received FDA 510(k) clearance on 1988-11-16, under 510(k) number K883236.

Who is the listed applicant for CEFAR DUAL?

The FDA 510(k) record lists Cefar Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CEFAR DUAL?

The FDA product code for CEFAR DUAL is GZJ.

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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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