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FDA 510(k)

KERR CAVALITE

K-Number: K872147 · 1987-08-26

ApplicantKerr Corporation (Danbury)
Decision Date1987-08-26
Product CodeEJK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KERR CAVALITE 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 1987-08-26 under 510(k) number K872147. The device is classified under product code EJK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KERR CAVALITE?

KERR CAVALITE is a medical device that received FDA 510(k) clearance on 1987-08-26. The listed applicant is Kerr Corporation (Danbury). The 510(k) number is K872147.

When did KERR CAVALITE receive FDA 510(k) clearance?

KERR CAVALITE received FDA 510(k) clearance on 1987-08-26, under 510(k) number K872147.

Who is the listed applicant for KERR CAVALITE?

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 KERR CAVALITE?

The FDA product code for KERR CAVALITE is EJK.

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Other records listing Kerr Corporation (Danbury) as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: EJK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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