510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K072362Substantially Equivalent

Novalung Surgical Lung Assist (Sla) Membrane Lung

Novalung GmbH, North Attleboro MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072362 is the FDA 510(k) clearance record for NOVALUNG SURGICAL LUNG ASSIST (SLA) MEMBRANE LUNG, a class II device, cleared for Novalung GmbH on under FDA product code DTZ (Oxygenator, Cardiopulmonary Bypass). FDA records list 2 510(k) clearances for Novalung GmbH, from to . As of , FDA records show no recalls naming K072362.

Clearance record

Decision date
Received
(62 days to decision)
Product code
DTZ Oxygenator, Cardiopulmonary Bypass
Regulation
21 CFR 870.4350
Device class
Class II
Review panel
Cardiovascular
Applicant
Novalung GmbH 49 Plain St., North Attleboro MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DTZ

Trailing 12 months
5 clearances under product code DTZ in the twelve months to October 2026, March 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code DTZ, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20262
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260