510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K873012Substantially Equivalent

Infant Cannula

Gresco International, Inc., San Antonio TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873012 is the FDA 510(k) clearance record for INFANT CANNULA, a class II device, cleared for Gresco International, Inc. on under FDA product code DQR (Cannula, Catheter). FDA records list one 510(k) clearance for Gresco International, Inc. As of , FDA records show no recalls naming K873012.

Clearance record

Decision date
Received
(272 days to decision)
Product code
DQR Cannula, Catheter
Regulation
21 CFR 870.1300
Device class
Class II
Review panel
Cardiovascular
Applicant
Gresco International, Inc. P.O. Box 690188, San Antonio TX
Third party review
No

Clearances, product code DQR

Trailing 12 months

FDA records hold no clearances under product code DQR in the trailing twelve months.

FDA records show no clearances under product code DQR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DQR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260