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

P2020-8-0 BEAM-LIMITING DEVICE

K Number: K914184 · Decision Nov 27, 1991
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
15
Applicant Total
13
Review Days
70

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Basic Information

Device Name
P2020-8-0 BEAM-LIMITING DEVICE
K Number
K914184
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1610
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Precise Optics
Date Received
September 18, 1991
Decision Date
November 27, 1991
Product Code
KPW
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
KPW Device, Beam Limiting, X-Ray, Diagnostic

Similar 510(k) Clearances

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Other Clearances by Precise Optics

K Number Device Name
K030061 PS 3000 DIGATAL PHOTOSPOT SYSTEM
K935580 PHF20 20 MOBILE C-ARM IMAGE INTENSIFIER
K932878 PRECISION INTRA-ORAL SCOPES
K914084 ENDOSCOPES
K911744 PRECISION OPTICS CORPORATION LAPAROSCOPE
K903459 PRECISION OPTICS ENDOSCOPE ADAPTER
K903457 PRECISION OPTICS IMAGE BEAMSPLITTER (COUPLER)
K903458 PRECISION OPTICS IMAGE COUPLER
K820178 PI808 MOBILE C-ARM IMAGE INTENSIFIER
K827087 P1808 MOBILE C-ARM IMAGE INTENSIFIER
Search all 13 clearances from Precise Optics →