BYO · Class I · 21 CFR 868.5220

FDA Product Code BYO: Bottle, Blow

Leading manufacturers include Travenol Laboratories, S.A., B & F Medical Products, Inc. and Kist Intl..

4

Total

4

Cleared

137d

Avg days

1978

Since

FDA 510(k) Cleared Bottle, Blow Devices (Product Code BYO)

4 devices

1–4 of 4

Cleared Jul 09, 1993

EPIDURAL MINIPACK

Anesthesiology · 304d

Cleared Jan 21, 1992

Anesthesiology · 166d

Cleared May 26, 1978

BOTTLE BREATHING DEVICE

B & F Medical Products, Inc.

Anesthesiology · 51d

Cleared Apr 10, 1978

2C7125 BLOW BOTTLE

Travenol Laboratories, S.A.

Anesthesiology · 28d

About Product Code BYO - Regulatory Context

Related FDA 510(k) Regulatory Insights

Data Source

FDA 510(k) public files . 176,583 total devices indexed.

Latest clearance: Jul 09, 1993

Product Code Info

Code	BYO
Device class	Class I
CFR	21 CFR 868.5220
Panel	Anesthesiology

Verify on FDA.gov

View BYO classification on FDA.gov →