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FDA 510(k)

MODIFICATION TO RELIEF BRIEF

K-Number: K003128 · 2002-08-12

ApplicantThe JM Kohn Co.
Decision Date2002-08-12
Product CodeNJB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO RELIEF BRIEF is the device name listed in this FDA 510(k) record. The listed applicant is The JM Kohn Co.. It received FDA 510(k) clearance on 2002-08-12 under 510(k) number K003128. The device is classified under product code NJB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO RELIEF BRIEF?

MODIFICATION TO RELIEF BRIEF is a medical device that received FDA 510(k) clearance on 2002-08-12. The listed applicant is The JM Kohn Co.. The 510(k) number is K003128.

When did MODIFICATION TO RELIEF BRIEF receive FDA 510(k) clearance?

MODIFICATION TO RELIEF BRIEF received FDA 510(k) clearance on 2002-08-12, under 510(k) number K003128.

Who is the listed applicant for MODIFICATION TO RELIEF BRIEF?

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

What is the FDA product code for MODIFICATION TO RELIEF BRIEF?

The FDA product code for MODIFICATION TO RELIEF BRIEF is NJB.

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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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