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

HUMID-VENT FILTER PEDI

K Number: K952084 · Decision Jun 12, 1995
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
72
Applicant Total
15
Review Days
40

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Basic Information

Device Name
HUMID-VENT FILTER PEDI
K Number
K952084
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Gibeck, Inc.
Date Received
May 3, 1995
Decision Date
June 12, 1995
Product Code
BYD
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
BYD Condenser, Heat And Moisture (Artificial Nose)

Similar 510(k) Clearances

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Other Clearances by Gibeck, Inc.

K Number Device Name
K965016 ISO-GARD FILTER ANGLED(18212)/ISO-GARD FILTER STRAIGHT(19212)
K964377 THERMAL REGULATION SYSTEM BLANKET
K964382 HUMID-VENT FILTER COMPACT ANGLED (18402)/HUMID-VENT FILTER COMPACT STRAIGHT(19402)
K960511 GIBECK WARMBAG REUSABLE CONVECTIVE WARMING BLANKET
K954828 ISO-GARD HEPA FILTER-HME, ISO-ARD HEPA FILTER-HME W/PORT
K953544 HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHT
K953491 HUMID-VENT 1 PORT/HUMID-VENT 1 PORT ANGLE
K952845 HUMID-VENT TRACH-VENT
K952844 HUMID-VENT 2
K952750 HUMID-VENT 1
Search all 15 clearances from Gibeck, Inc. →