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FDA 510(k)

PNEUMOTHORAX KIT, MODIFICATION

K-Number: K904021 · 1990-10-09

ApplicantArrow Intl., Inc.
Decision Date1990-10-09
Product CodeJDC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PNEUMOTHORAX KIT, MODIFICATION 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 1990-10-09 under 510(k) number K904021. The device is classified under product code JDC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PNEUMOTHORAX KIT, MODIFICATION?

PNEUMOTHORAX KIT, MODIFICATION is a medical device that received FDA 510(k) clearance on 1990-10-09. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K904021.

When did PNEUMOTHORAX KIT, MODIFICATION receive FDA 510(k) clearance?

PNEUMOTHORAX KIT, MODIFICATION received FDA 510(k) clearance on 1990-10-09, under 510(k) number K904021.

Who is the listed applicant for PNEUMOTHORAX KIT, MODIFICATION?

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 PNEUMOTHORAX KIT, MODIFICATION?

The FDA product code for PNEUMOTHORAX KIT, MODIFICATION is JDC.

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Related Devices (Code: JDC)

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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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