510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K083842Substantially Equivalent

Rotem Delta Thromboelastometry System

Pentapharm AG, Munich, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K083842 is the FDA 510(k) clearance record for ROTEM DELTA THROMBOELASTOMETRY SYSTEM, a class II device, cleared for Pentapharm GmbH on under FDA product code JPA (System, Multipurpose For In Vitro Coagulation Studies). FDA records list 3 510(k) clearances for Pentapharm GmbH, from to . As of , FDA records show 2 recalls naming K083842.

Clearance record

Decision date
Received
(454 days to decision)
Product code
JPA System, Multipurpose For In Vitro Coagulation Studies
Regulation
21 CFR 864.5425
Device class
Class II
Review panel
Hematology
Applicant
Pentapharm GmbH Stahlgruberring 12, Munich, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JPA

Trailing 12 months
1 clearance under product code JPA in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JPA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260