FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DISPOSABLE ARACHNOID KNIFE

K Number: K882422 · Decision Sep 6, 1988
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
33
Applicant Total
13
Review Days
85

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DISPOSABLE ARACHNOID KNIFE
K Number
K882422
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
882.4535
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Microbio-Medics, Inc.
Date Received
June 13, 1988
Decision Date
September 6, 1988
Product Code
HAO
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
HAO Instrument, Surgical, Non-Powered

Similar 510(k) Clearances

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

View all

Other Clearances by Microbio-Medics, Inc.

K Number Device Name
K923353 VENTILATION TUBES W/ HYDROGEL COATING
K922572 321Q MINIMUM ENERGY TINNITUS SUPPRESSOR
K913276 MICROTEK MEDICAL'S SOUND STIKS
K904239 SOFT HYDROXYLAPATITE OSSICULAR MALLEABLE PROSTHES
K910167 MICROTEK-HERITAGES SILICONE BULB EVACUATION SYSTEM
K900726 MICROTEK MEDICAL'S BLOOD COLLECTION KIT
K901154 MICROTEK'S SURGICAL LAMP HANDLE & COVER
K895815 MICROTEK TOTAL OSSICULAR PROTHESIS
K895814 MICROTEK PISTON & WIRE PROSTHESES
K895502 MICROTEK REUTER-STYLE BI-VALVE INTRANASAL SPLINT
Search all 13 clearances from Microbio-Medics, Inc. →