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

MEDICAL EXAM TABLE

K Number: K830294 · Decision Jan 11, 1984
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
13
Applicant Total
20
Review Days
349

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Basic Information

Device Name
MEDICAL EXAM TABLE
K Number
K830294
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4960
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Coe Laboratories, Inc.
Date Received
January 27, 1983
Decision Date
January 11, 1984
Product Code
LGX
Advisory Committee
General, Plastic Surgery
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
LGX Table, Examination, Medical, Powered

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K Number Device Name
K903292 ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS
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K894281 FIRST IMPRESSION WITH CHLORHEXIDINE
K891140 OCCLU-SEAL(TM) VISIBLE LIGHT-CURED FISSURE SEALANT
K885010 TRIPTON(TM) VISIBLE LIGHT-CURED UNIV. BONDING
K881422 COE PAK AUTO MIX, REGULAR OR HARD SET
K881091 OMNISIL, VINYL POLYSILOXANE IMPRESSION MATERIAL
K863882 OPALUX VISIBLE LIGHT CURED ANTERIOR COMPOSITE
K842877 ABSOLUTE VINYL POLYSILOXANE IMPRESS
K844325 COE-LITE POLYMERIZATION UNIT
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