510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K880637Substantially Equivalent

Baxter, Pharmaseal Patient Gas Sampling Lines

Baxter Healthcare Corporation, Valencia CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K880637 is the FDA 510(k) clearance record for BAXTER, PHARMASEAL PATIENT GAS SAMPLING LINES, a class I device, cleared for Baxter Healthcare Corp on under FDA product code BZO (Set, Tubing And Support, Ventilator (W Harness)). FDA records list 570 510(k) clearances for Baxter Healthcare Corp, from to . As of , FDA records show no recalls naming K880637.

Clearance record

Decision date
Received
(55 days to decision)
Product code
BZO Set, Tubing And Support, Ventilator (W Harness)
Regulation
21 CFR 868.5975
Device class
Class I
Review panel
Anesthesiology
Applicant
Baxter Healthcare Corp 27200 N. Tourney Rd., Valencia CA
Third party review
No

Clearances, product code BZO

Trailing 12 months

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

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