THAYER METERED DOSE INHALER DISPENSER/ADAPTER— 510(k) K901739

Name: FDA 510(k) clearance K901739
Creator: U.S. Food and Drug Administration
Published: 1990-10-09

Substantially Equivalent

Thayer Medical Corp.

FDA 510(k) clearance K901739 for THAYER METERED DOSE INHALER DISPENSER/ADAPTER, Substantially Equivalent on 1990-10-09. Applicant: Thayer Medical Corp.. Device class: 1.

Clearance details

Applicant: Thayer Medical Corp.
Product code: Code CAI
Device class: Class 1
Regulation: 21 CFR 868.5240
Advisory panel: Anesthesiology
Date received: 1990-04-16
Decision date: 1990-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucson, AZ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CAI

view all

K954480 — CONDENSATE COLLECTION KIT1995-12-29
K953787 — UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUIT1995-09-19
K953788 — UNICOR, INC. GAS SAMPLING LINES & CONNECTORS1995-09-19
K952014 — PRIMA ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS1995-05-22
K952016 — PRIMA PEDIATRIC GAS SAMPLING CIRCUITS1995-05-22

More clearances from Thayer Medical Corp.

view all

K102658 — MINISPACER DUAL-SPRAY MDI ADAPTER WITH 22MM (OR 15MM) OD / 22MM OD/ID CONNECTIONS / 15MM ID CONNECTIONS2010-12-10
K993101 — LITEAIRE2000-10-26
K992722 — PRIMEAIRE1999-11-10
K972237 — HAND HELD MEDISPACER1997-07-31
K955805 — DUAL SPRAY MINISPACER1996-03-21

Adverse events under product code CAI

product code CAI

Malfunction: 869
Other: 1
Total: 870

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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