510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K880740Substantially Equivalent

Model Ta-Cs10 Spectraject Control Syringe

Spectramed, LLC, Oxnard CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K880740 is the FDA 510(k) clearance record for MODEL TA-CS10 SPECTRAJECT CONTROL SYRINGE, a class II device, cleared for Spectramed, Inc. on under FDA product code DQF (Actuator, Syringe, Injector Type). FDA records list 20 510(k) clearances for Spectramed, Inc., from to . As of , FDA records show no recalls naming K880740.

Clearance record

Decision date
Received
(27 days to decision)
Product code
DQF Actuator, Syringe, Injector Type
Regulation
21 CFR 870.1670
Device class
Class II
Review panel
Cardiovascular
Applicant
Spectramed, Inc. 1900 Williams Dr., Oxnard CA
Third party review
No

Clearances, product code DQF

Trailing 12 months

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

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