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FDA 510(k)

ARROW PNEUMOTHORAX KIT, AK-01500

K-Number: K883905 · 1989-01-19

ApplicantArrow Intl., Inc.
Decision Date1989-01-19
Product CodeJOL
Advisory CommitteeHO
DecisionUnknown

Device Summary

ARROW PNEUMOTHORAX KIT, AK-01500 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 1989-01-19 under 510(k) number K883905. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ARROW PNEUMOTHORAX KIT, AK-01500?

ARROW PNEUMOTHORAX KIT, AK-01500 is a medical device that received FDA 510(k) clearance on 1989-01-19. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K883905.

When did ARROW PNEUMOTHORAX KIT, AK-01500 receive FDA 510(k) clearance?

ARROW PNEUMOTHORAX KIT, AK-01500 received FDA 510(k) clearance on 1989-01-19, under 510(k) number K883905.

Who is the listed applicant for ARROW PNEUMOTHORAX KIT, AK-01500?

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 ARROW PNEUMOTHORAX KIT, AK-01500?

The FDA product code for ARROW PNEUMOTHORAX KIT, AK-01500 is JOL.

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Related Devices (Code: JOL)

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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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