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FDA 510(k)

KEITH-A.R.V.

K-Number: K851444 · 1985-05-10

ApplicantKarl M. Block Co.
Decision Date1985-05-10
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KEITH-A.R.V. is the device name listed in this FDA 510(k) record. The listed applicant is Karl M. Block Co.. It received FDA 510(k) clearance on 1985-05-10 under 510(k) number K851444. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEITH-A.R.V.?

KEITH-A.R.V. is a medical device that received FDA 510(k) clearance on 1985-05-10. The listed applicant is Karl M. Block Co.. The 510(k) number is K851444.

When did KEITH-A.R.V. receive FDA 510(k) clearance?

KEITH-A.R.V. received FDA 510(k) clearance on 1985-05-10, under 510(k) number K851444.

Who is the listed applicant for KEITH-A.R.V.?

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

What is the FDA product code for KEITH-A.R.V.?

The FDA product code for KEITH-A.R.V. is KNT.

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Related Devices (Code: KNT)

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

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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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