Atlas FDA

ESPE CAPMIX

FDA 510(k) clearance K891064 · decided 1989-05-30

Clearance details

K-number
K891064
Device name
ESPE CAPMIX
Applicant
Espe GmbH (Us)
Decision
Substantially Equivalent
Date received
1989-03-01
Decision date
1989-05-30
Days to decision
90 days
Clearance type
Traditional
Product code
EFD
Device class
1
Regulation number
872.3100
Medical specialty
Dental
Advisory committee
Dental
Location
Lake Worth, FL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
PENTAMIX 2 (K991913)Espe Dental AG1999-07-26
SILIMAT PLUS (K923974)Ivoclar North America, Inc.1992-10-06
IPT CAPSULE MIXER (K922203)Ipt Technologies, Inc.1992-06-03
AUTOMIX DENTAL AMALGAMATOR (K915847)Kerr Corporation (Danbury)1992-03-02
DUOMAT 3 AMALGAMATOR (K914340)Degussa AG1991-11-13
MIXOMAT AMALGAMATOR (K914341)Degussa AG1991-11-13
DENTOMAT 3 AMALGAMATORS (K914339)Degussa AG1991-11-07
ACCU-MIX AMALGAMATOR (K910632)Wykle Research, Inc.1991-03-15
SILAMAT (AMALGAMATOR) (K901909)Ivoclar North America, Inc.1990-06-22
DRILLING MACHINE W/HANDPIECES & INTERNAL IRRIGA. (K891612)Implant Innovations International, Inc.1989-06-12
AMALGAMATOR (K880993)Acecodent, Inc.1988-05-11
AMALGAMATOR MODEL SDC-- (K791410)Sierra Laboratories, Inc.1979-09-19

Recalls involving this device

No recalls on record reference this clearance.