Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Everest Medical Corp. · Predicate Candidate Screening

21 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

79 daysmedian FDA review time
153 days90th percentile
21clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K003060PLASMAKINETIC GENERATOREverest Medical Corp.2000-10-31290
K000496EVERSHEARS BIPOLAR SCISSORSEverest Medical Corp.2000-04-24690
K993412BITX PROBESEverest Medical Corp.2000-03-311710
K994336BITX PROBESEverest Medical Corp.2000-02-08470
K971565BICOAG COAGULATING FORCEPSEverest Medical Corp.1998-03-123170
K955001EVERSHEARS SCISSORS, BILAP PROBES, BICOAG FORCEPSEverest Medical Corp.1995-12-13410
K945975EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPSEverest Medical Corp.1994-12-21130
K922509LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRAEverest Medical Corp.1992-10-011270
K922246TUBING SET W/ IRRIGATION & ASPIRATION VALVINGEverest Medical Corp.1992-09-021120
K920089MONOPOLAR COAGULATING POLYPECTOMY SNAREEverest Medical Corp.1992-03-31830
K911787MONOPOLAR SPHINCTERTOMEEverest Medical Corp.1991-07-19880
K911700MONOPOLAR POLLYPECTOMY SNAREEverest Medical Corp.1991-07-01760
K912544BIPOLAR FORCEPSEverest Medical Corp.1991-06-24140
K905714ERCP CANNULAEverest Medical Corp.1991-02-01420
K904985BIPOLAR BIOPSY FORCEPSEverest Medical Corp.1991-01-25840
K904993LAPAROSCOPIC ELECTROSURGICAL DEVICEEverest Medical Corp.1991-01-25790
K895842BITOME(TM) BIPOLAR SPHINCTEROTOMEEverest Medical Corp.1990-01-111010
K895841MODEL 8750 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENE.Everest Medical Corp.1989-11-15440
K892895MODEL 8800 BIPOLAR COAGULATION THERAPEUTIC SYSTEMEverest Medical Corp.1989-09-251530
K893553BIPOLAR ELECTROSURGICAL SNAREEverest Medical Corp.1989-09-081230
K870981MODEL 8700 BIPOLAR ELECTROSURGICAL GENERATOREverest Medical Corp.1987-05-06570

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda