HUMID-VENT 2 S FLEX— 510(k) K881656

Substantially Equivalent

Gibeck Respiration

FDA 510(k) clearance K881656 for HUMID-VENT 2 S FLEX, Substantially Equivalent on 1988-06-16. Applicant: Gibeck Respiration. Device class: 1.

Clearance details

Applicant: Gibeck Respiration
Product code: Code BYD
Device class: Class 1
Regulation: 21 CFR 868.5375
Advisory panel: Anesthesiology
Date received: 1988-04-15
Decision date: 1988-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Schaumburg, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BYD

K955008 — HEAT & MOISTURE EXCHANGER1996-01-30
K954194 — DISPOSABLE HME/FILTER1995-10-20
K953580 — HEAT MOISTURE EXCHANGER1995-09-15
K953507 — TYPE 1 & 2 (HUMIDAIR I & II)1995-09-07
K953491 — HUMID-VENT 1 PORT/HUMID-VENT 1 PORT ANGLE1995-08-25

More clearances from Gibeck Respiration

K881657 — HUMID-VENT FILTER1988-06-24
K881644 — HUMID-VENT 2 S1988-06-10
K873768 — HUMID-VENT(R) 2 PORT1987-11-24
K873767 — HUMID-VENT(R) MINI1987-11-06
K872153 — STOM-VENT1987-08-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.