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

Stethoscope Head

21 CFR 868.1930 / Anesthesiology
FDA source (opens on fda.gov)

BZS is the FDA product code for Stethoscope Head, a class I device type, regulated under 21 CFR 868.1930. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
BZS
Device name
Stethoscope Head
Regulation
21 CFR 868.1930
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
3
Ingested recalls
0

Clearances, product code BZS

By decision year
3 clearances under product code BZS with a decision year between 1980 and 1994, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code BZS by decision year
YearClearances
19801
19931
19941

Applicants with the most clearances

Product code BZS
Applicants holding the most 510(k) clearances under product code BZS
ApplicantClearances
Modern Medical Devices, Inc.1
Nova Diversified Concepts1
Warner-Lambert Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 21 companies shown, in name order