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

NEZHAT-DORSEY SPECIMEN CONTAINER SYSTEM

K Number: K951119 · Decision Jun 13, 1995
Classifications
1
FEI Numbers
193
Registration Numbers
193
Same Product Code
86
Applicant Total
18
Review Days
95

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Basic Information

Device Name
NEZHAT-DORSEY SPECIMEN CONTAINER SYSTEM
K Number
K951119
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
American Hydro-Surgical Instruments, Inc.
Date Received
March 10, 1995
Decision Date
June 13, 1995
Product Code
GCX
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered

Similar 510(k) Clearances

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

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Other Clearances by American Hydro-Surgical Instruments, Inc.

K Number Device Name
K953574 NEZHAT-DORSEY HYDRO-DISSECTION UNIVERSAL BAG SQUEEZER
K953481 NEZHAT-DORSEY HYDRO-DISSECTION UNIVERSAL BAGSQUEEZER
K952070 NEZHAT-DORSEY ELECTROSURGICAL HAND CONTROL ATTACHMENTS, PENCIL-GRIP HANDLES & TRUMPET VALVE W/CUTTING & COAGULATION HANS
K946380 NEZHAT-DORSEY REUSABLE ASPIRATION-VAC PROBES WITH AND WITHOUT PUNCTURE CANNULA (HEREINAFTER REFERRED TO AS ASPIRATION-V)
K951300 NEZHAT-DORSEY THERMAL RETENTION SYSTEM
K950499 NEZHAT-DORSEY LAPAROSCOPIC HAND INSTRUMENTS
K952421 NEZHAT-DORSEY REUSABLE UNIPOLAR COAGULATOR PROBE INSERTS
K951733 NEXHAT-DORSEY PENCIL-GRIP TRUMPET VALVE WITH CUTTING AND COAGULATION HAND CONTROLS
K951732 NEZHAT-DORESEY PENCIL-GRIP HANDLES
K951731 NEZHAT-DORESY ELECTROSURGICAL HAND CONTROL ATTACHMENTS
Search all 18 clearances from American Hydro-Surgical Instruments, Inc. →