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FDA 510(k)

POSITIVE PLACEMENT ANETHESIA KIT

K-Number: K781469 · 1979-01-26

ApplicantArrow Intl., Inc.
Decision Date1979-01-26
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

POSITIVE PLACEMENT ANETHESIA KIT is the device name listed in this FDA 510(k) record. The listed applicant is Arrow Intl., Inc.. It received FDA 510(k) clearance on 1979-01-26 under 510(k) number K781469. 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 POSITIVE PLACEMENT ANETHESIA KIT?

POSITIVE PLACEMENT ANETHESIA KIT is a medical device that received FDA 510(k) clearance on 1979-01-26. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K781469.

When did POSITIVE PLACEMENT ANETHESIA KIT receive FDA 510(k) clearance?

POSITIVE PLACEMENT ANETHESIA KIT received FDA 510(k) clearance on 1979-01-26, under 510(k) number K781469.

Who is the listed applicant for POSITIVE PLACEMENT ANETHESIA KIT?

The FDA 510(k) record lists Arrow Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POSITIVE PLACEMENT ANETHESIA KIT?

The FDA product code for POSITIVE PLACEMENT ANETHESIA KIT is CAZ.

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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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