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FDA 510(k)

ANESTHESIA KIT, EPIDURAL BLOCK, CONTINU.

K-Number: K770461 · 1977-03-16

ApplicantArrow Intl., Inc.
Decision Date1977-03-16
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA KIT, EPIDURAL BLOCK, CONTINU. 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 1977-03-16 under 510(k) number K770461. 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 BLOCK, CONTINU.?

ANESTHESIA KIT, EPIDURAL BLOCK, CONTINU. is a medical device that received FDA 510(k) clearance on 1977-03-16. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K770461.

When did ANESTHESIA KIT, EPIDURAL BLOCK, CONTINU. receive FDA 510(k) clearance?

ANESTHESIA KIT, EPIDURAL BLOCK, CONTINU. received FDA 510(k) clearance on 1977-03-16, under 510(k) number K770461.

Who is the listed applicant for ANESTHESIA KIT, EPIDURAL BLOCK, CONTINU.?

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 BLOCK, CONTINU.?

The FDA product code for ANESTHESIA KIT, EPIDURAL BLOCK, CONTINU. is 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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