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Machida Endoscope Co., Ltd.

Abiko Chiba, JP

MACHIDA ENDOSCOPE CO., LTD. appears in FDA device records in Abiko Chiba, JP. FDA records list one 510(k) clearance, 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) clearances
1
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 1 510(k) clearance for Machida Endoscope Co., Ltd. in 2000.

Clearances by year, as a table
510(k) clearance decisions for Machida Endoscope Co., Ltd., by decision year
YearClearances
20001
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K993568MACHIDA FLEXIBLE NEURO-ENDOSCOPE, MODELS NEU-4, NEU-4LGWGSubstantially Equivalent

Registered establishments

FDA registered establishments for Machida Endoscope Co., Ltd., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
96812463002807522MACHIDA ENDOSCOPE CO., LTD.15-12 Abiko 1 Chome, Abiko Chiba 270-1166 JP2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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