510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K941790Substantially Equivalent

Pro-Tect Safety Dressing

Pro-Tect Medical Products, Inc., Eden Prairie MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K941790 is the FDA 510(k) clearance record for PRO-TECT SAFETY DRESSING, cleared for Pro-Tect Medical Products, Inc. on under FDA product code MGP (Dressing, Wound And Burn, Occlusive). FDA records list 2 510(k) clearances for Pro-Tect Medical Products, Inc. As of , FDA records show no recalls naming K941790.

Clearance record

Decision date
Received
(276 days to decision)
Product code
MGP Dressing, Wound And Burn, Occlusive
Device class
Unclassified
Review panel
Unknown
Applicant
Pro-Tect Medical Products, Inc. 9905 Hamilton Rd., Eden Prairie MN
510(k) summary
Summary
Third party review
No

Clearances, product code MGP

Trailing 12 months

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

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