510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K242820Substantially Equivalent

Puritan PurSafe Plus Collection and Transport System

Puritan Medical Products Company, LLC, Guilford ME / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K242820 is the FDA 510(k) clearance record for Puritan PurSafe Plus Collection and Transport System, a class II device, cleared for Puritan Medical Products, LLC on under FDA product code QBD (Microbial Nucleic Acid Storage And Stabilization Device). FDA's definition for product code QBD reads: "Molecular transport media is a device intended for the stabilization and transportation of nucleic acids from unprocessed human samples suspected of containing infectious material". FDA records list 8 510(k) clearances for Puritan Medical Products, LLC, from to . As of , FDA records show no recalls naming K242820.

Clearance record

Decision date
Received
(251 days to decision)
Product code
QBD Microbial Nucleic Acid Storage And Stabilization Device
Regulation
21 CFR 866.2950
Device class
Class II
Review panel
Microbiology
Applicant
Puritan Medical Products, LLC 31 School St., P.O. Box 149, Guilford ME
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QBD

Trailing 12 months

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

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