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

RATE INCREASE FOR IPPB/IPV

K Number: K896586 · Decision Jan 9, 1990
Classifications
1
FEI Numbers
112
Registration Numbers
112
Same Product Code
7
Applicant Total
11
Review Days
48

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Basic Information

Device Name
RATE INCREASE FOR IPPB/IPV
K Number
K896586
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.5410
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Percussionaire Corp.
Date Received
November 22, 1989
Decision Date
January 9, 1990
Product Code
DZD
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
DZD Tube, Orthodontic

Similar 510(k) Clearances

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

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Other Clearances by Percussionaire Corp.

K Number Device Name
K905234 TXP TRANSPORTER FAMILY AND RELATED ACCESSORIES
K905235 VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS
K905236 IPV PERCUSSIONATOR FAMILY & RELATED ACCESSORIES
K900315 PERCUSSIONAIRE TXP TRANSPORTER/RESPIRATORS 750 MIN
K900314 PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN
K900313 PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN
K895485 BIRD (IPV) NONCONTINUOUS VENTILATORS
K892886 PERCUSSIONAIRE OSCILLATRON-1 MEDICAL RESPIRATOR
K895486 BIRD (VDR) SINUSOIDAL PERCUSSIONATORS
K884832 PERCUSSIONAIRE RESPIRATORS (MULTIPLE)
Search all 11 clearances from Percussionaire Corp. →