CAMClass I

Yoke Assembly, Medical Gas

21 CFR 868.6885 / Anesthesiology

CAM is the FDA product code for Yoke Assembly, Medical Gas, a class I device type, regulated under 21 CFR 868.6885. As of 2026-09-10, FDA records hold 8 510(k) clearances under this code, the most recent dated 1994-03-11, and no recalls.

Classification record

Product code: CAM
Device name: Yoke Assembly, Medical Gas
Regulation: 21 CFR 868.6885
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: 8
Ingested recalls: 0

Clearances, product code CAM

By decision year

8 clearances under product code CAM with a decision year between 1977 and 1994, 1985 the highest year at 4.

Show the numbers

510(k) clearances under FDA product code CAM by decision year
Year	Clearances
1977	1
1978	1
1984	1
1985	4
1994	1

Applicants with the most clearances

Product code CAM

Applicants holding the most 510(k) clearances under product code CAM
Applicant	Clearances
Penox Technologies, Inc.	4
American Gage & Medical, Inc.	1
Bel-Med, Inc	1
Siemens Elema AB	1
Spica, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 20 companies shown, in name order