CALClass I

Laryngoscope, Non-Rigid

21 CFR 868.5530 / Anesthesiology

CAL is the FDA product code for Laryngoscope, Non-Rigid, a class I device type, regulated under 21 CFR 868.5530. As of 2026-09-10, FDA records hold 8 510(k) clearances under this code, the most recent dated 1995-04-06, and 11 recalls.

Classification record

Product code: CAL
Device name: Laryngoscope, Non-Rigid
Regulation: 21 CFR 868.5530
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: 11

Clearances, product code CAL

By decision year

8 clearances under product code CAL with a decision year between 1979 and 1995, 1980 the highest year at 2.

Show the numbers

510(k) clearances under FDA product code CAL by decision year
Year	Clearances
1979	1
1980	2
1985	2
1988	1
1995	2

Applicants with the most clearances

Product code CAL

Applicants holding the most 510(k) clearances under product code CAL
Applicant	Clearances
American Optical Corp.	3
Pentax Precision Instrument Corp.	2
Haemonetics Corporation	1
Olympus Corp.	1
Reichert-Jung, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 55 companies shown, in name order