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

OXY-VAC

K Number: K842205 · Decision Jun 25, 1984
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
115
Applicant Total
36
Review Days
21

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Basic Information

Device Name
OXY-VAC
K Number
K842205
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6810
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Medi-Tech, Inc.
Date Received
June 4, 1984
Decision Date
June 25, 1984
Product Code
BSY
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
BSY Catheters, Suction, Tracheobronchial

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Other Clearances by Medi-Tech, Inc.

K Number Device Name
K954457 MEDI-TECH EDDY INTRAVASCULAR INFUSION CATHETER
K952345 MEDI-TECH PLATFORM GUIDE CATHETER
K952056 IMMUNOASSAY DRUGS OF ABUSE CONTROLS
K945289 DOA - IMMUNOASSAY CUT-OFF CALIBRATOR
K942551 THERAPEUTIC DRUG MONITORING CONTROL, ASSAYED
K943290 BILIRUBIN PLUS/PEDIATRIC CONTROLS
K922990 HEMODIALYSIS BATH
K942552 THERAPEUTIC DRUG MONITORING CONTROL, UNASSAYED
K904073 COAGULATION REFERENCE PLASMA, ABNORMAL
K895819 MODIFIED LABELING TO THE SPAND-GEL GRANULATED GEL
Search all 36 clearances from Medi-Tech, Inc. →