510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K014115Substantially Equivalent

1St Response Manual Resuscitator, Model 85Xx

Abbott Medical, Keene NH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K014115 is the FDA 510(k) clearance record for 1ST RESPONSE MANUAL RESUSCITATOR, MODEL 85XX, a class II device, cleared for Portex, Inc. on under FDA product code BTM (Ventilator, Emergency, Manual (Resuscitator)). FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show 3 recalls naming K014115.

Clearance record

Decision date
Received
(75 days to decision)
Product code
BTM Ventilator, Emergency, Manual (Resuscitator)
Regulation
21 CFR 868.5915
Device class
Class II
Review panel
Anesthesiology
Applicant
Portex, Inc. 10 Bowman Dr., Keene NH
510(k) summary
Summary
Third party review
No

Clearances, product code BTM

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