510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K913726Substantially Equivalent

Duralife(tm)

Dhd Diemolding Healthcare Div., Canastota NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913726 is the FDA 510(k) clearance record for DURALIFE(TM), a class I device, cleared for Dhd Diemolding Healthcare Div. on under FDA product code BZA (Connector, Airway (Extension)). FDA records list 11 510(k) clearances for Dhd Diemolding Healthcare Div., from to . As of , FDA records show no recalls naming K913726.

Clearance record

Decision date
Received
(171 days to decision)
Product code
BZA Connector, Airway (Extension)
Regulation
21 CFR 868.5810
Device class
Class I
Review panel
Anesthesiology
Applicant
Dhd Diemolding Healthcare Div. 125 Rasbach St., Canastota NY
510(k) summary
Statement
Third party review
No

Clearances, product code BZA

Trailing 12 months

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

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