510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K780407Substantially Equivalent

2C7125 Blow Bottle

Travenol Laboratories, S.A., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K780407 is the FDA 510(k) clearance record for 2C7125 BLOW BOTTLE, a class I device, cleared for Travenol Laboratories, S.A. on under FDA product code BYO (Bottle, Blow). FDA records list 206 510(k) clearances for Travenol Laboratories, S.A., from to . As of , FDA records show no recalls naming K780407.

Clearance record

Decision date
Received
(28 days to decision)
Product code
BYO Bottle, Blow
Regulation
21 CFR 868.5220
Device class
Class I
Review panel
Anesthesiology
Applicant
Travenol Laboratories, S.A. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code BYO

Trailing 12 months

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

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