510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K033054Substantially Equivalent

Harvard 1 Syringe Pump/harvard 1 with Pca Syringe Pump

Harvard Clinical Technology, South Natick MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K033054 is the FDA 510(k) clearance record for HARVARD 1 SYRINGE PUMP/HARVARD 1 WITH PCA SYRINGE PUMP, a class II device, cleared for Harvard Clinical Technology on under FDA product code MEA (Pump, Infusion, Pca). FDA records list 2 510(k) clearances for Harvard Clinical Technology, from to . As of , FDA records show 2 recalls naming K033054.

Clearance record

Decision date
Received
(78 days to decision)
Product code
MEA Pump, Infusion, Pca
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Harvard Clinical Technology 22 Pleasant St., South Natick MA
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code MEA

Trailing 12 months

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

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