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

MICRO-INGRESSOR HANDIPIECE

K Number: K954796 · Decision Nov 6, 1995
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
90
Applicant Total
14
Review Days
19

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Basic Information

Device Name
MICRO-INGRESSOR HANDIPIECE
K Number
K954796
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4250
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Trebay Medical Corp.
Date Received
October 18, 1995
Decision Date
November 6, 1995
Product Code
ERL
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
ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece

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Other Clearances by Trebay Medical Corp.

K Number Device Name
K955704 TREBAY MICRODEBRIDER SYSTEM
K955560 TREBAY SCOPE IRRIGATED CLEARING SLEEVE
K955294 SOF - ABRASION BUR
K955447 TYMPANOSTOMY TUBE
K954912 TREBAY IRRIGATED CUTTER BLADE (MODIFICATION)
K954795 AT2 & DOYLE STYLE (C-FLEX) VENT TUBES
K954517 TREBAY PARTIAL RECTRANGULAR HEADS, MORETZ CAM, INCUS/STAPEDIAL JOINT & STRAIGHT INCUS STRUT
K954518 TREBAY TOTAL RECTANGULAR HEAD
K954715 MICRO-PLANER HANDPIECE
K952226 C-FLEX SEPTAL SPLINTS
Search all 14 clearances from Trebay Medical Corp. →