FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BIOPSY FORCEPS

K Number: K895415 · Decision Oct 31, 1989
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
238
Applicant Total
34
Review Days
56

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Basic Information

Device Name
BIOPSY FORCEPS
K Number
K895415
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4680
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Symbiosis Corp.
Date Received
September 5, 1989
Decision Date
October 31, 1989
Product Code
EOQ
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EOQ Bronchoscope (Flexible Or Rigid)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EOQ), ordered by most recent decision date.

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Other Clearances by Symbiosis Corp.

K Number Device Name
K955119 SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES
K953453 SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES
K953242 SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES
K952432 SYMBIOSIS BIPOLAR FORCEPS
K951387 SYMBIOSIS BIPOLAR SCISSORS
K950286 SYMBIOSIS BIPOLAR SCISSORS
K946238 SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPS
K930773 SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS
K941426 SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE
K932266 SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN
Search all 34 clearances from Symbiosis Corp. →