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

MANUAL CHAIR BASE

K Number: K921027 · Decision Mar 20, 1992
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
63
Applicant Total
11
Review Days
17

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Basic Information

Device Name
MANUAL CHAIR BASE
K Number
K921027
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3920
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Labac Systems, Inc.
Date Received
March 3, 1992
Decision Date
March 20, 1992
Product Code
KNN
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
KNN Components, Wheelchair

Similar 510(k) Clearances

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

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Other Clearances by Labac Systems, Inc.

K Number Device Name
K941157 BASIC RECLINE CHAIR
K934418 BASIC TILT CHAIR ( BTC )
K932639 MANUAL TILT RECLINE CHAIR (MTC)
K923362 REDUCED SHEAR OWR RECLINE SYSTEM
K923363 ADJUSTABLE SLIDING BACK POWER RECLINE SYSTEM
K921028 MANUAL RECLINING CHAIR
K923364 TILT ADJUSTABLE SLIDING BACK RECLINE SEATING SYST
K923366 TILT SEATING SYSTEM
K925272 PEDIATRIC TILT CHAIR
K921136 MANUAL TILT CHAIR
Search all 11 clearances from Labac Systems, Inc. →