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Grieshaber & Co.

Fallisington, PA, US

Grieshaber & Co. appears in FDA device records in Fallisington, PA. FDA records list 15 510(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
15
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 15 510(k) clearances for Grieshaber & Co. between 1986 and 1995. The busiest year on record is 1986, with 4. The most recent is 1995, with 1.

Clearances by year, as a table
510(k) clearance decisions for Grieshaber & Co., by decision year
YearClearances
19864
19881
19892
19902
19924
19941
19951
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K950056THE GRIESHABER AXIAL CUTTERHKPSubstantially Equivalent
K930842THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGEHQESubstantially Equivalent
K914588GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGEGAWSubstantially Equivalent
K914587GRIESHABER AIR/FLUID TUBING SETKYGSubstantially Equivalent
K914586GRIESHABER THREE FUNCTION MANIPULATOREQHSubstantially Equivalent
K914585GRIESHABER TWO FUNCTION MANIPULATOREQHSubstantially Equivalent
K897119GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEPHQWSubstantially Equivalent
K900714ZZIPP INSTANT BOVIE CLEANERGEISubstantially Equivalent
K890782GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES)HMXSubstantially Equivalent
K890783GRIESHABER VISCOELASTIC INJECTION SYSTEMFRNSubstantially Equivalent
K884043GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGEHQESubstantially Equivalent
K864056GRIESHABER AIR SYSTEM/PRESSURE OPHTHALMIC IRRIGANTHQCSubstantially Equivalent
K863444GRIESHABER GLOBAL CONTROL TUBING SETHQCSubstantially Equivalent
K860479GREEN-LINE BIPOLAR COAGULATION UNITGEISubstantially Equivalent
K860502G.A.S./GRIESHABER AIR SYSTEMFRNSubstantially 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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What MDM checks, and what it does not

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