510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K801173Substantially Equivalent

Angio-Flo Monitoring Kit

Hospital Products Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K801173 is the FDA 510(k) clearance record for ANGIO-FLO MONITORING KIT, a class II device, cleared for Hospital Products Co. on under FDA product code KRA (Catheter, Continuous Flush). FDA records list 6 510(k) clearances for Hospital Products Co., from to . As of , FDA records show no recalls naming K801173.

Clearance record

Decision date
Received
(12 days to decision)
Product code
KRA Catheter, Continuous Flush
Regulation
21 CFR 870.1210
Device class
Class II
Review panel
Cardiovascular
Applicant
Hospital Products Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KRA

Trailing 12 months
5 clearances under product code KRA in the twelve months to October 2026, September 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KRA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20261
July 20260
August 20260
September 20262
October 20260