ARROW JUGULAR PUNCTURE KIT 16 GA.— 510(k) K820009

Substantially Equivalent

Arrow Intl., Inc.

FDA 510(k) clearance K820009 for ARROW JUGULAR PUNCTURE KIT 16 GA., Substantially Equivalent on 1982-01-22. Applicant: Arrow Intl., Inc.. Device class: 2.

Clearance details

Applicant
Arrow Intl., Inc.
Product code
Code DQY
Device class
Class 2
Regulation
21 CFR 870.1250
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code DQY

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More clearances from Arrow Intl., Inc.

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Adverse events under product code DQY

product code DQY
Death
464
Injury
4,489
Malfunction
13,721
Other
2
Total
18,676

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K820009

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K820009.

Data sourced from openFDA. This site is unofficial and independent of the FDA.