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Apmtd, Inc.

Wilmington, MA, US

APMTD, INC. appears in FDA device records in Wilmington, MA. FDA records list 2 510(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) clearances
2
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 2 510(k) clearances for Apmtd, Inc. in 2023.

Clearances by year, as a table
510(k) clearance decisions for Apmtd, Inc., by decision year
YearClearances
20232
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K230698Anivia SG1000 Pump ConsoleDWASubstantially Equivalent
K221491Anivia SG1000 Pump ConsoleDWASubstantially Equivalent

Registered establishments

FDA registered establishments for Apmtd, Inc., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30154316383015431638APMTD, INC.226 Lowell Street, Wilmington, MA 01887 US2026

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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What MDM checks, and what it does not

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