510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K880923Substantially Equivalent

Patient Ventilator Isolator

Dryden Corp., Indianapolis IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K880923 is the FDA 510(k) clearance record for PATIENT VENTILATOR ISOLATOR, a class II device, cleared for Dryden Corp. on under FDA product code CBK (Ventilator, Continuous, Facility Use). FDA records list 21 510(k) clearances for Dryden Corp., from to . As of , FDA records show no recalls naming K880923.

Clearance record

Decision date
Received
(186 days to decision)
Product code
CBK Ventilator, Continuous, Facility Use
Regulation
21 CFR 868.5895
Device class
Class II
Review panel
Anesthesiology
Applicant
Dryden Corp. 10640 E. 59th St., Indianapolis IN
Third party review
No

Clearances, product code CBK

Trailing 12 months
4 clearances under product code CBK in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CBK, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20261
April 20261
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260