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

PROBE

K Number: K841624 · Decision Aug 27, 1984
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
13
Review Days
130

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Basic Information

Device Name
PROBE
K Number
K841624
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Plastafil, Inc.
Date Received
April 19, 1984
Decision Date
August 27, 1984
Product Code
HRX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HRX Arthroscope

Similar 510(k) Clearances

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

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Other Clearances by Plastafil, Inc.

K Number Device Name
K841621 BACK RADIUS CUTTER
K841620 FRONT RADIUS CUTTER
K841617 STROVER HOOK
K841629 DRILL BIT
K841625 HOOK
K841618 THREADING TUBE
K841626 PUNCH
K841627 MALLET
K841628 WIRE
K841622 SOFT-TISSUE INSTRUMENT
Search all 13 clearances from Plastafil, Inc. →