510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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MetriTrack, Inc.

Oak Brook, IL, US

MetriTrack, Inc. appears in FDA device records in Oak Brook, IL. 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 MetriTrack, Inc. between 2014 and 2021. The busiest year on record is 2014, with 1. The most recent is 2021, with 1.

Clearances by year, as a table
510(k) clearance decisions for MetriTrack, Inc., by decision year
YearClearances
20141
20211
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K211098Breast Volume Navigator (BVN) Model G-2000IYOSubstantially Equivalent
K141870BREAST VOLUME NAVIGATORIYNSubstantially Equivalent

Registered establishments

FDA registered establishments for MetriTrack, Inc., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30114113093011411309MetriTrack, Inc.1010 Jorie Blvd Ste 48, Oak Brook, IL 60523 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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Data as of , FDA export datePage updated Source: openFDA, public domain