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FDA 510(k)

ARROW JUGULAR PUNCTURE KIT 16 GA.

K-Number: K820009 · 1982-01-22

ApplicantArrow Intl., Inc.
Decision Date1982-01-22
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARROW JUGULAR PUNCTURE KIT 16 GA. 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 1982-01-22 under 510(k) number K820009. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARROW JUGULAR PUNCTURE KIT 16 GA.?

ARROW JUGULAR PUNCTURE KIT 16 GA. is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K820009.

When did ARROW JUGULAR PUNCTURE KIT 16 GA. receive FDA 510(k) clearance?

ARROW JUGULAR PUNCTURE KIT 16 GA. received FDA 510(k) clearance on 1982-01-22, under 510(k) number K820009.

Who is the listed applicant for ARROW JUGULAR PUNCTURE KIT 16 GA.?

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 JUGULAR PUNCTURE KIT 16 GA.?

The FDA product code for ARROW JUGULAR PUNCTURE KIT 16 GA. is DQY.

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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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