510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K910926Substantially Equivalent

Tecnadyne Surgi-Squeeze Infusion Pump

Tecnadyne Scientific, Inc., Vero Beach FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K910926 is the FDA 510(k) clearance record for TECNADYNE SURGI-SQUEEZE INFUSION PUMP, a class I device, cleared for Tecnadyne Scientific, Inc. on under FDA product code KZD (Infusor, Pressure, For I.V. Bags). FDA records list 5 510(k) clearances for Tecnadyne Scientific, Inc., from to . As of , FDA records show no recalls naming K910926.

Clearance record

Decision date
Received
(150 days to decision)
Product code
KZD Infusor, Pressure, For I.V. Bags
Regulation
21 CFR 880.5420
Device class
Class I
Review panel
General Hospital
Applicant
Tecnadyne Scientific, Inc. 740 C Fourteenth St., Vero Beach FL
Third party review
No

Clearances, product code KZD

Trailing 12 months

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

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