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FDA 510(k)

CURITY PARACERVICAL/PUDENDAL BLOCK ANES

K-Number: K801724 · 1980-08-07

ApplicantThe Kendal Co.
Decision Date1980-08-07
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CURITY PARACERVICAL/PUDENDAL BLOCK ANES 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 1980-08-07 under 510(k) number K801724. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY PARACERVICAL/PUDENDAL BLOCK ANES?

CURITY PARACERVICAL/PUDENDAL BLOCK ANES is a medical device that received FDA 510(k) clearance on 1980-08-07. The listed applicant is The Kendal Co.. The 510(k) number is K801724.

When did CURITY PARACERVICAL/PUDENDAL BLOCK ANES receive FDA 510(k) clearance?

CURITY PARACERVICAL/PUDENDAL BLOCK ANES received FDA 510(k) clearance on 1980-08-07, under 510(k) number K801724.

Who is the listed applicant for CURITY PARACERVICAL/PUDENDAL BLOCK ANES?

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 PARACERVICAL/PUDENDAL BLOCK ANES?

The FDA product code for CURITY PARACERVICAL/PUDENDAL BLOCK ANES is CAZ.

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Other records listing The Kendal Co. as applicant

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Related Devices (Code: CAZ)

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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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