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Mega Electronics, Ltd.

The Hague, NL

Mega Electronics , Ltd. appears in FDA device records in The Hague, NL. FDA records list 4 510(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
4
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 4 510(k) clearances for Mega Electronics, Ltd. between 1997 and 2015. The busiest year on record is 1997, with 1. The most recent is 2015, with 1.

Clearances by year, as a table
510(k) clearance decisions for Mega Electronics, Ltd., by decision year
YearClearances
19971
20001
20131
20151
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K143032eMotion Faros ECG MobileDXHSubstantially Equivalent
K131699EMOTION ECG MOBILEDXHSubstantially Equivalent
K993411FEMISCAN CLINIC SYSTEM, MODEL FS-ICTRA AND FEMISCAN PERSONAL SYSTEM, MODEL FS-HMTRHIRSubstantially Equivalent
K963202MEGA ME 3000 PROFESSIONAL MUSCLE TESTERHCCSubstantially 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.

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What MDM checks, and what it does not

MDM coverage

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