Device Classification Name |
forceps, biopsy, electric |
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---|---|---|---|---|
510(k) Number | K992390 | |||
Device Name | HOT BIOPSY FORCEPS FEENESTRATED 230 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATED 160 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATD | |||
Applicant |
|
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Applicant Contact | john a chaves | |||
Correspondent |
|
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Correspodent Contact | john a chaves | |||
Regulation Number | 876.4300 | |||
Classification Product Code |
|
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Date Received | 07/19/1999 | |||
Decision Date | 12/22/1999 | |||
Decision |
substantially equivalent (SESE) |
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Regulation Medical Specialty |
Gastroenterology/Urology |
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510k Review Panel |
Gastroenterology/Urology |
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statement |
statement |
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Type | Traditional | |||
Reviewed by Third Party | No | |||
Combination Product |
No |