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

SAFETY DRAIN

K Number: K881790 · Decision Jun 21, 1988
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
21
Applicant Total
26
Review Days
56

Basic Information

Device Name
SAFETY DRAIN
K Number
K881790
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5995
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
BALLARD MEDICAL PRODUCTS
Date Received
April 26, 1988
Decision Date
June 21, 1988
Product Code
BYH
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
BYH Drain, Tee (Water Trap)

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