FDA 510(k)

TEMP BOND NE

K-Number: K894219 · 1989-09-18

Decision Date1989-09-18

Product CodeEMA

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

TEMP BOND NE is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corporation (Danbury). It received FDA 510(k) clearance on 1989-09-18 under 510(k) number K894219. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMP BOND NE?

TEMP BOND NE is a medical device that received FDA 510(k) clearance on 1989-09-18. The listed applicant is Kerr Corporation (Danbury). The 510(k) number is K894219.

When did TEMP BOND NE receive FDA 510(k) clearance?

TEMP BOND NE received FDA 510(k) clearance on 1989-09-18, under 510(k) number K894219.

Who is the listed applicant for TEMP BOND NE?

The FDA 510(k) record lists Kerr Corporation (Danbury) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEMP BOND NE?

The FDA product code for TEMP BOND NE is EMA.

Other records listing Kerr Corporation (Danbury) as applicant

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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.