510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
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K802101Substantially Equivalent

i.v. Sentry Alarm Device

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

K802101 is the FDA 510(k) clearance record for I.V. SENTRY ALARM DEVICE, a class II device, cleared for Pike Medical Co. on under FDA product code FLN (Monitor, Electric For Gravity Flow Infusion Systems). FDA records list one 510(k) clearance for Pike Medical Co. As of , FDA records show no recalls naming K802101.

Clearance record

Decision date
Received
(13 days to decision)
Product code
FLN Monitor, Electric For Gravity Flow Infusion Systems
Regulation
21 CFR 880.2420
Device class
Class II
Review panel
General Hospital
Applicant
Pike Medical Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FLN

Trailing 12 months

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

FDA records show no clearances under product code FLN in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FLN, 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