Atlas FDA

THERMO ELECTRON ANGIOTENSIN CONVERTING ENZYME INFINITY (ACE) REAGENT

FDA 510(k) clearance K041657 · decided 2004-08-30

Clearance details

K-number
K041657
Device name
THERMO ELECTRON ANGIOTENSIN CONVERTING ENZYME INFINITY (ACE) REAGENT
Applicant
Thermo Electron Corporation
Decision
Substantially Equivalent
Date received
2004-06-18
Decision date
2004-08-30
Days to decision
73 days
Clearance type
Traditional
Product code
KQN
Device class
2
Regulation number
862.1090
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Louisville, CO, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Thermo Electron Corporation

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
ANGIOTENSIN CONVERTING ENZYME REA (K942497)American Laboratory Products Co., Ltd.1994-11-15
BUEHLMANN LAB AS, ACE ANGIO CONV ENZYME KIN ASSAY (K913091)American Laboratory Products Co., Ltd.1991-08-26
ALDOSTERONE DIRECT RIA KIT (K854876)Biotecx Laboratories, Inc.1986-03-17
SIGMA ANGIOTENSIN CONVERTING ENZYME 305-UV (K854245)Sigma Diagnostics, Inc.1986-01-22
ACE COLOR TEST (K833933)Hana Biologics, Inc.1984-03-23
ACE ACTIVITY MICROVIAL TEST SET (K821011)Ventrex Laboratories, Inc.1982-05-03
ANGIOTENSIN CONVERTING ENZYME ASSAY SYS (K791712)Ventrex Laboratories, Inc.1979-09-19

Recalls involving this device

No recalls on record reference this clearance.