Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Clinical Technology Corp. — Predicate Candidate Screening

12 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

90 daysmedian FDA review time

351 days90th percentile

12clearances measured

K-number	Device	Applicant	Decided	Review days	Recalls (K-match)
K925080	TEK-LUBE	Clinical Technology Corp.	1994-01-31	481	0
K872867	BIOSIGN	Clinical Technology Corp.	1988-07-06	351	0
K880166	BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000	Clinical Technology Corp.	1988-02-18	35	0
K872705	BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT)	Clinical Technology Corp.	1987-09-01	56	0
K855138	BOVIE ULTRASONIC SURGICAL SYSTEM	Clinical Technology Corp.	1986-11-10	322	0
K854231	ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES	Clinical Technology Corp.	1986-05-02	193	0
K853507	STERI-GRIP	Clinical Technology Corp.	1985-09-05	15	0
K852986	GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN	Clinical Technology Corp.	1985-08-19	35	0
K844565	BOVIE X-10 ELECTROSURGICAL GENERATOR(UNIT)	Clinical Technology Corp.	1985-02-21	90	0
K841272	SICKLE-STAT HEMOGLOBIN S SCREEN KIT	Clinical Technology Corp.	1984-04-13	17	1
K823077	URINARY BLADDER TEMP. SENSOR #81-003	Clinical Technology Corp.	1983-03-09	141	0
K813000	DISPOSABLE ARTHROSCOPY CANNULA SET	Clinical Technology Corp.	1982-01-22	88	0

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda