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

THE GNATHOMETER-M

K Number: K810972 · Decision May 5, 1981
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
1
Applicant Total
11
Review Days
26

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Basic Information

Device Name
THE GNATHOMETER-M
K Number
K810972
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.3150
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Bauer, Cheng & Associates, Inc.
Date Received
April 9, 1981
Decision Date
May 5, 1981
Product Code
KZO
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
KZO Ink, Arch Tracing

Similar 510(k) Clearances

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Other Clearances by Bauer, Cheng & Associates, Inc.

K Number Device Name
K840084 COLTENE BRILLIANT LUX
K840085 COLTENE BRILLIANT
K823098 REX-CAPS
K823100 RX 91
K823097 NATURELLE
K823099 RX MIDACAST
K823084 CHALLENGER
K810970 ISOSIT TEETH
K810971 THE GNATOMET
K810969 ISOSIT C & B MATERIAL
Search all 11 clearances from Bauer, Cheng & Associates, Inc. →