The following data is part of a premarket notification filed by Airlife, Inc. with the FDA for Two-piece I.p.p.b. Manifold-with Right.
Device ID | K792030 |
510k Number | K792030 |
Device Name: | TWO-PIECE I.P.P.B. MANIFOLD-WITH RIGHT |
Classification | Set, Tubing And Support, Ventilator (w Harness) |
Applicant | AIRLIFE, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | BZO |
CFR Regulation Number | 868.5975 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-10-09 |
Decision Date | 1979-10-30 |