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Dymax Corp

Pittsburgh, PA, US

Dymax Corp appears in FDA device records in Pittsburgh, PA. FDA records list 7 510(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
7
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 7 510(k) clearances for Dymax Corp between 1985 and 2003. The busiest year on record is 1985, with 1. The most recent is 2003, with 1.

Clearances by year, as a table
510(k) clearance decisions for Dymax Corp, by decision year
YearClearances
19851
19861
19891
19901
19931
19991
20031
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K032135SITE-RITE IV ULTRASOUND SYSTEMIYOSubstantially Equivalent
K993624SITE-RITE 3 ULTRASOUND SYSTEMIYOSubstantially Equivalent
K931403SITERITE NEEDLE GUIDE (MODIFIED)DQYSubstantially Equivalent
K903158SITERITE NEEDLE GUIDEDQYSubstantially Equivalent
K894415DYMAX ENDOVAGINAL BIOPSY GUIDEHGLSubstantially Equivalent
K862127DYMAX PERSONAL SCANNERIYOSubstantially Equivalent
K850478PLUS 1IYOSubstantially 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

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