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

VITACOMM 100 ESOPHAGEAL STETHOSCOPE

K Number: K842309 · Decision Jun 22, 1984
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
45
Applicant Total
2
Review Days
10

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Basic Information

Device Name
VITACOMM 100 ESOPHAGEAL STETHOSCOPE
K Number
K842309
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1920
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Vitacomm, Inc.
Date Received
June 12, 1984
Decision Date
June 22, 1984
Product Code
BZT
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BZT Stethoscope, Esophageal, With Electrical Conductors

Similar 510(k) Clearances

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

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Other Clearances by Vitacomm, Inc.

K Number Device Name
K885347 VITACOMM MODEL #140/141 ESOPHAGEAL STETHOSCOPE