510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K760082Substantially Equivalent

Bottle, Condensate (#1628)

Inspiron Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K760082 is the FDA 510(k) clearance record for BOTTLE, CONDENSATE (#1628), a class II device, cleared for Inspiron Corp. on under FDA product code CBC (Bottle, Collection And Trap, Breathing System (Uncalibrated)). FDA records list 20 510(k) clearances for Inspiron Corp., from to . As of , FDA records show no recalls naming K760082.

Clearance record

Decision date
Received
(25 days to decision)
Product code
CBC Bottle, Collection And Trap, Breathing System (Uncalibrated)
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Applicant
Inspiron Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CBC

Trailing 12 months

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

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