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FDA 510(k)

CURITY ANESTHESIA FILTER

K-Number: K864103 · 1987-01-28

ApplicantThe Kendal Co.
Decision Date1987-01-28
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CURITY ANESTHESIA FILTER is the device name listed in this FDA 510(k) record. The listed applicant is The Kendal Co.. It received FDA 510(k) clearance on 1987-01-28 under 510(k) number K864103. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY ANESTHESIA FILTER?

CURITY ANESTHESIA FILTER is a medical device that received FDA 510(k) clearance on 1987-01-28. The listed applicant is The Kendal Co.. The 510(k) number is K864103.

When did CURITY ANESTHESIA FILTER receive FDA 510(k) clearance?

CURITY ANESTHESIA FILTER received FDA 510(k) clearance on 1987-01-28, under 510(k) number K864103.

Who is the listed applicant for CURITY ANESTHESIA FILTER?

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

What is the FDA product code for CURITY ANESTHESIA FILTER?

The FDA product code for CURITY ANESTHESIA FILTER is CAH.

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Other records listing The Kendal Co. 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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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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