510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K970255Substantially Equivalent

Kipp Med i.v. Manifold

The Kipp Group, Ontario CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K970255 is the FDA 510(k) clearance record for KIPP MED I.V. MANIFOLD, a class II device, cleared for The Kipp Group on under FDA product code FPA (Set, Administration, Intravascular). FDA records list 6 510(k) clearances for The Kipp Group, from to . As of , FDA records show no recalls naming K970255.

Clearance record

Decision date
Received
(82 days to decision)
Product code
FPA Set, Administration, Intravascular
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Applicant
The Kipp Group 930 Wanamaker Ave., Ontario CA
510(k) summary
Summary
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