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

BONE GRAFT DELIVERY SYRINGES

K Number: K941431 · Decision Jul 12, 1994
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
12
Applicant Total
17
Review Days
110

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Basic Information

Device Name
BONE GRAFT DELIVERY SYRINGES
K Number
K941431
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bio-Interfaces, Inc.
Date Received
March 24, 1994
Decision Date
July 12, 1994
Product Code
EID
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
EID Syringe, Restorative And Impression Material

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Other Clearances by Bio-Interfaces, Inc.

K Number Device Name
K960164 BIO-INTERFACES, INC., BIORESORBABLE CALCIUM PHOSPHATE PARTICLES - BII-GRAFT 6140
K954763 BIO-INTERFACES, INC,. BII-PLAST
K950598 BIORESORBABLE CALCIUM PHOSPHATE PARTICLES - BLL-GRAFT
K950567 BIO-APATITE 6140 HA PARTICLES
K950511 BLL-FIL 6140 PARTICLES
K934049 BII-PORE(TM) CANAL WALL PROSTHESIS
K933688 BII-PORE
K934430 BON APATITE HA PARTICLES
K934947 BII-PLAST
K924287 710 POROUS HA PARTICLES-BII-PORE
Search all 17 clearances from Bio-Interfaces, Inc. →