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

RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT

K Number: K882244 · Decision Jun 23, 1988
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
14
Applicant Total
71
Review Days
23

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Basic Information

Device Name
RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT
K Number
K882244
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.5800
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Richards Medical Co., Inc.
Date Received
May 31, 1988
Decision Date
June 23, 1988
Product Code
EPP
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
EPP Splint, Nasal

Similar 510(k) Clearances

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Other Clearances by Richards Medical Co., Inc.

K Number Device Name
K896106 ROGOZINSKI SPINAL SYSTEM, ADD'L COMPONENTS
K900628 MODULAR HIP SYSTEM
K896580 UNI-POLAR HEAD
K895241 INTRAMEDULLARY HIP SCREW
K884824 TRICON-M TOTAL KNEE SYSTEM
K896204 ZIRCONIA CERAMIC HEAD ADD'L SIZES
K895242 PAPPAS TRI-FLANGE VENTILATION TUBE
K893377 RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS
K885069 ZIRCONIA CERAMIC HEAD (YITRIA STABILIZED)
K892366 POROUS GENESIS STEMMED TIBIAL COMPONENT
Search all 71 clearances from Richards Medical Co., Inc. →