BZAClass I

Connector, Airway (Extension)

21 CFR 868.5810 / Anesthesiology

BZA is the FDA product code for Connector, Airway (Extension), a class I device type, regulated under 21 CFR 868.5810. As of 2026-09-10, FDA records hold 94 510(k) clearances under this code, the most recent dated 2009-03-05, and 38 recalls.

Classification record

Product code: BZA
Device name: Connector, Airway (Extension)
Regulation: 21 CFR 868.5810
Device class: Class I
Review panel: Anesthesiology
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 94
Ingested recalls: 38

Clearances, product code BZA

By decision year

94 clearances under product code BZA with a decision year between 1977 and 2009, 1986 the highest year at 14.

Show the numbers

510(k) clearances under FDA product code BZA by decision year
Year	Clearances
1977	5
1978	2
1979	10
1980	1
1981	10
1983	2
1984	1
1985	4
1986	14
1987	4
1988	6
1989	5
1991	4
1992	6
1993	6
1994	8
1995	5
2009	1

Applicants with the most clearances

Product code BZA

Applicants holding the most 510(k) clearances under product code BZA
Applicant	Clearances
Airlife, Inc.	11
Dhd Medical Products Div. Diemolding Corp.	8
Intersurgical Ltd.	4
Dhd Diemolding Healthcare Div.	3
Intertech/Ohio	3
Prima, Inc.	3
Acutronic Medical Systems AG	2
B & B Medical Technologies, Inc.	2
Hospitak, Inc.	2
Instrumentation Industries, Incorporated	2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 150 companies shown, in name order