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

MODEL 902 STAND

K Number: K780759 · Decision May 19, 1978
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
7
Applicant Total
22
Review Days
11

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Basic Information

Device Name
MODEL 902 STAND
K Number
K780759
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Applied Medical Research
Date Received
May 8, 1978
Decision Date
May 19, 1978
Product Code
FSH
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FSH Tray, Surgical, Needle

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Other Clearances by Applied Medical Research

K Number Device Name
K800025 DINAMAP RESEARCH MONITOR 1245
K791580 CEREBRAL FUNCTION MONITOR 870
K791159 DINAMAP MODEL 855
K790322 OPTIONAL ACCESSORY FOOT SWITCH MODEL 100
K790328 MODEL 1051, MONITOR
K782073 DINAMAP MODELS 1160 AND 1165
K781053 DINAMAP MODEL 846
K781064 DINAMAP MODEL 848
K781311 ELECTRODE, NEEDLE, CFM
K780754 NEONATAL MONITOR
Search all 22 clearances from Applied Medical Research →