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

BELMONT AUTOPAN-PANORAMIC 098 CEPHALOMETRIC-RADIOG

K Number: K844554 · Decision Feb 21, 1985
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
33
Applicant Total
12
Review Days
92

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Basic Information

Device Name
BELMONT AUTOPAN-PANORAMIC 098 CEPHALOMETRIC-RADIOG
K Number
K844554
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1840
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Belmont Equipment Corp.
Date Received
November 21, 1984
Decision Date
February 21, 1985
Product Code
IWZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
IWZ Film, Radiographic

Similar 510(k) Clearances

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

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Other Clearances by Belmont Equipment Corp.

K Number Device Name
K000799 BELMONT UNIT, MODEL 2000 SERIES
K983661 BELMONT UNIT, MODEL 6000 SERIES AND 7500 SERIES
K963699 BELRAY/MODEL 096, DENTAL INTRAORAL X-RAY
K900681 PANORAMIC MODEL X-CALIBER X-RAY
K874238 MODEL 2001 CP, PHOTON I, DENTAL, INTRAORAL X-RAY
K870300 BELMONT, PODIATRY X-RAY - REMEX, MODEL PD75
K861328 NEW BELMONT MODEL, MC-5 DENTAL, INTRAORAL X-RAY
K852019 BELMONT AUTOPAN-PAN ORAMIC, 098E CEPHALOMETRIC-RAD
K834279 ACURAY 071A DENTAL INTRAORAL X-RAY
K832065 ACURACY 071, DENTAL, INTRAORAL-X-RAY
Search all 12 clearances from Belmont Equipment Corp. →