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Cygnus, LLC

Paterson, NJ, US

Cygnus, LLC appears in FDA device records in Paterson, NJ. FDA records list one 510(k) clearance, no PMA records and no registered establishments. As of , FDA records show 2 recalls for this company.

FDA records held for this company

510(k) clearances
1
PMA records
0
Recall records
2
Registered establishments
0

510(k) clearance history

FDA records hold 1 510(k) clearance for Cygnus, LLC in 2008.

Clearances by year, as a table
510(k) clearance decisions for Cygnus, LLC, by decision year
YearClearances
20081
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K072950CYGNUS 12 LEAD ECG MODULEKRESubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

Device recall records naming this company, most recent first
RecallProductReasonClassificationInitiatedStatus
Z-0564-06Centrifuge Model CF-6 with lid lock. (Block Model Number OCT-VI). Units are distributed to Bloch Scientific, Holbrook, NY for Bloch''s customers MFT and Cascade.When device was packaged, too much expanding foam was added causing the lid to deform and causing the lid locking mechanism to be out of alignment.Terminated
Z-0563-06Centrifuge Model CF-6 with lid lock. (Block Model number OCT-VI). Units are distributed to Bloch Scientific, Holbrook, NY for Bloch''s customers MFT and Cascade.The units were exhibiting tolerance stacking in the electronic circuit timer that controls the electric motor that spins the centrifuge and applies the centrifuge brake.Terminated

Verification record

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