510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K903539Substantially Equivalent

Salter Labs Model #1015

Salter Labs, Arvin CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K903539 is the FDA 510(k) clearance record for SALTER LABS MODEL #1015, a class I device, cleared for Salter Labs on under FDA product code CBH (Device, Fixation, Tracheal Tube). FDA records list 74 510(k) clearances for Salter Labs, from to . As of , FDA records show no recalls naming K903539.

Clearance record

Decision date
Received
(132 days to decision)
Product code
CBH Device, Fixation, Tracheal Tube
Regulation
21 CFR 868.5770
Device class
Class I
Review panel
Anesthesiology
Applicant
Salter Labs P.O. Box 608, Arvin CA
Third party review
No

Clearances, product code CBH

Trailing 12 months

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

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