510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K884657Substantially Equivalent

Lily i.v. Set

Modec Co., Inc., San Jose CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K884657 is the FDA 510(k) clearance record for LILY I.V. SET, a class II device, cleared for Modec Co., Inc. on under FDA product code FPA (Set, Administration, Intravascular). FDA records list one 510(k) clearance for Modec Co., Inc. As of , FDA records show no recalls naming K884657.

Clearance record

Decision date
Received
(135 days to decision)
Product code
FPA Set, Administration, Intravascular
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Applicant
Modec Co., Inc. 405b Reynolds Cir., San Jose CA
Third party review
No

Clearances, product code FPA

Trailing 12 months
5 clearances under product code FPA in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FPA, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20261
June 20261
July 20260
August 20260
September 20261
October 20260