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

WALL MOUNTED LASER POSITIONING DEVICE

K Number: K801541 · Decision Aug 20, 1980
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
27
Applicant Total
17
Review Days
48

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Basic Information

Device Name
WALL MOUNTED LASER POSITIONING DEVICE
K Number
K801541
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.5780
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Advantage Medical Systems, Inc.
Date Received
July 3, 1980
Decision Date
August 20, 1980
Product Code
IWE
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
IWE Monitor, Patient Position, Light-Beam

Similar 510(k) Clearances

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Other Clearances by Advantage Medical Systems, Inc.

K Number Device Name
K873957 NON-CORING HUBER TYPE NEEDLES
K873290 LACERATION AND INSTRUMENT TRAYS
K863494 NEONATAL PHYSIOLOGICAL MONITOR MODEL PM 20
K861556 MODIFIED FETAL MONITOR MODEL FM-2
K861279 FLUORO PLUS
K861455 MODEL DT-102 DATA TELEPHONE TRANSMITTER
K852518 MODIFICATION FETAL MONITOR MODEL FM-2
K844724 FETAL TELEMETRY SYSTEM
K842462 HOLTER SCREENING MONITOR HS-221
K840747 TOCO DATA TELEPHONE TRANSMITTER DT100P
Search all 17 clearances from Advantage Medical Systems, Inc. →