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Cathlab Corp.

Tustin, CA, US

Cathlab Corp. appears in FDA device records in Tustin, CA. FDA records list 8 510(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
8
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 8 510(k) clearances for Cathlab Corp. between 1988 and 1991. The busiest year on record is 1991, with 3. The most recent is 1991, with 3.

Clearances by year, as a table
510(k) clearance decisions for Cathlab Corp., by decision year
YearClearances
19881
19892
19902
19913
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K910917CATHLAB SILICONE BILIARY BALLOON CATHETERGCASubstantially Equivalent
K910916CATHLAB SILICONE OCCLUSION BALLOON CATHETERDQTSubstantially Equivalent
K905139CATHLAB SILICONE ARTERIAL EMBOLECTOMY CATHETERDXESubstantially Equivalent
K897051MILLER PERCUTANEOUS ANGIOGRAPHIC/SCOPIC IRRI. CATHDQOSubstantially Equivalent
K8971843F AND 4F IRRIGATION EMBOLECTOMY CATHETERSDXESubstantially Equivalent
K893435SILICONE FLOW-DIRECTED THERMODILUTION CATHETERDYGSubstantially Equivalent
K893680SILICONE BI-LUMEN IRRIGATION EMBOLECTOMY CATH.DXESubstantially Equivalent
K881455EMBOLECTOMY CATHETER(MODIFIED)DXESubstantially 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