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510(k) Premarket Notification Database

510(k) Premarket Notification Database
Device Classification Name: TAPE, TELEVISION & VIDEO, ENDOSCOPIC
Regulation Number: 876.1500
[See Other Products with this regulation number]
510(k) Number: K032544
Device Name: VP-1000; MED CAM 100; VP-3000A; MED CAM 300
Applicant: MGB ENDOSKOPISCHE GERATE GMBH (BERLIN)
SCHWARZSCHILDSTRASSE 6

BERLIN,
Contact: J TSCHEPE
Product Code: FET
[See Other Manufacturers that make this Product]
Date Received: 08-18-2003
Decision Date: 09-02-2003
Decision: SE
Advisory Committee: GU
Statement/Summary/Purged Status: Summary
Type: Traditional
Review by Third Party: Y
Expedited Review: N
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