Clinical Technology Inc.
Brecksville, OH, US
CLINICAL TECHNOLOGY INC. appears in FDA device records in Brecksville, OH. FDA records list 12 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 12 510(k) clearances for Clinical Technology Inc. between 1982 and 1994. The busiest year on record is 1985, with 3. The most recent is 1994, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1982 | 1 |
| 1983 | 1 |
| 1984 | 1 |
| 1985 | 3 |
| 1986 | 2 |
| 1987 | 1 |
| 1988 | 2 |
| 1994 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K925080 | TEK-LUBE | EFB | Substantially Equivalent | |
| K872867 | BIOSIGN | FRC | Substantially Equivalent | |
| K880166 | BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000 | LFL | Substantially Equivalent | |
| K872705 | BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT) | GEI | Substantially Equivalent | |
| K855138 | BOVIE ULTRASONIC SURGICAL SYSTEM | LBK | Substantially Equivalent | |
| K854231 | ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES | GEI | Substantially Equivalent | |
| K853507 | STERI-GRIP | Substantially Equivalent | ||
| K852986 | GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN | LCP | Substantially Equivalent | |
| K844565 | BOVIE X-10 ELECTROSURGICAL GENERATOR(UNIT) | GEI | Substantially Equivalent | |
| K841272 | SICKLE-STAT HEMOGLOBIN S SCREEN KIT | GHM | Substantially Equivalent | |
| K823077 | URINARY BLADDER TEMP. SENSOR #81-003 | FLL | Substantially Equivalent | |
| K813000 | DISPOSABLE ARTHROSCOPY CANNULA SET | LXH | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1528657 | 1000136416 | CLINICAL TECHNOLOGY INC. | 7005 S Edgerton Rd, Brecksville, OH 44141 US | 2026 | No device listings on this registration |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- LCPAssay, Glycosylated Hemoglobin
- FLLContinuous Measurement Thermometer
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- EFBHandpiece, Air-Powered, Dental
- FRCIndicator, Biological Sterilization Process
- LFLInstrument, Ultrasonic Surgical
- LBKNeurosurgical Ultrasonic Instruments
- LXHOrthopedic Manual Surgical Instrument
- GHMTest, Sickle Cell
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Clinical Technology Inc. edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
Data as of , FDA export datePage updated Source: openFDA, public domain