Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR

Mediatech, Inc.

Washington, DC, US

Mediatech, Inc. appears in FDA device records in Washington, DC. FDA records list 24 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
24
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 24 510(k) clearances for Mediatech, Inc. between 1985 and 1986. The busiest year on record is 1985, with 23. The most recent is 1986, with 1.

Clearances by year, as a table
510(k) clearance decisions for Mediatech, Inc., by decision year
YearClearances
198523
19861
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K860623CELLGRO HEPES BUFFER SOLUTIONKITSubstantially Equivalent
K854567PENICILLIN/STREPTOMYCIN SOLUTIONKITSubstantially Equivalent
K852603MCCOY'S 5A MEDIUM - POWDERED FORMSubstantially Equivalent
K852602MCCOY'S 5A MEDIUM-LIQUID FORMKITSubstantially Equivalent
K852485CELLGRO(ISCOVE'S MEDIUM) MODIFICATIONKITSubstantially Equivalent
K852475CELLGRO WILLIAMS' MEDIUM EKITSubstantially Equivalent
K852288CELLGROKITSubstantially Equivalent
K850510EMEM W/NEAA-MINIMUM ESSENTIAL MED. W/NON-ESS. AMINKITSubstantially Equivalent
K850526EBSS W/O CA & MG-EARLE'S BALANCED SALT SOLUTIONKITSubstantially Equivalent
K850525DPBS-DULBECCO'S PHOSPHATE BUFFERED SALINEKITSubstantially Equivalent
K850524HBSS-HANKS' BALANCED SALT SOLUTIONKITSubstantially Equivalent
K850523EBSS-EARLE'S BALANCE SALT SOLUTIONKITSubstantially Equivalent
K850522MEM VITAMINS-MINIMUM ESSENTIAL MEDIUM VITAMINSKITSubstantially Equivalent
K850521MEM AA-MINIMUM ESSENTIAL MEDIUM AMINO ACIDSKITSubstantially Equivalent
K850520NEAA-NON-ESSENTIAL AMINO ACIDSKITSubstantially Equivalent
K850519GLUTAMINE-1-GLUTAMINEKITSubstantially Equivalent
K850518NA PYRUVATE-SODIUM PYRUVATEKITSubstantially Equivalent
K850517MED. 199 W/EARLE'S SALTS-MEDIUM 199 W/EARLES SALTSKITSubstantially Equivalent
K850516HAM'S F-12-A SPEDIFIC FORMULATION FORM DR. HAMKITSubstantially Equivalent
K850515HAM'S F-10-A SPEC. FORMULATION FROM DR. HAMKITSubstantially Equivalent
K850514ALPHA MEM-ALPHA MINIMUM ESSENTIAL MED. W/O RIBOSIDKITSubstantially Equivalent
K850513RPMI 1640-ROSWELL PARK MEMORIAL INSTITUTE 1640KITSubstantially Equivalent
K850512DMEM-DULBECCO'S MINIMUM ESSENTIAL MEDIUMKITSubstantially Equivalent
K850511EMEM-EARLE'S MINIMUM ESSENTIAL MED. W/GLUTAMINE-EAKITSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

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.

What MDM checks, and what it does not

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 Mediatech, Inc. edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.

The self-serve claim needs an FDA establishment registration, FEI or owner-operator number on the company’s record, and we hold none for Mediatech, Inc.. The only route for a company with no identifier on record is a person here: write to us, and one looks at the record and sends the same claim link by hand.

Data as of , FDA export datePage updated Source: openFDA, public domain