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FDA 510(k)

ANESTHESIA KIT, EPIDURAL, SINGLE SHOT

K-Number: K770356 · 1977-03-01

ApplicantArrow Intl., Inc.
Decision Date1977-03-01
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA KIT, EPIDURAL, SINGLE SHOT 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 1977-03-01 under 510(k) number K770356. 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 ANESTHESIA KIT, EPIDURAL, SINGLE SHOT?

ANESTHESIA KIT, EPIDURAL, SINGLE SHOT is a medical device that received FDA 510(k) clearance on 1977-03-01. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K770356.

When did ANESTHESIA KIT, EPIDURAL, SINGLE SHOT receive FDA 510(k) clearance?

ANESTHESIA KIT, EPIDURAL, SINGLE SHOT received FDA 510(k) clearance on 1977-03-01, under 510(k) number K770356.

Who is the listed applicant for ANESTHESIA KIT, EPIDURAL, SINGLE SHOT?

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 ANESTHESIA KIT, EPIDURAL, SINGLE SHOT?

The FDA product code for ANESTHESIA KIT, EPIDURAL, SINGLE SHOT 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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