Atlas FDA

DENTIMEDIC DENTAL EMERGENCY KIT

FDA 510(k) clearance K861681 · decided 1986-09-23

Clearance details

K-number
K861681
Device name
DENTIMEDIC DENTAL EMERGENCY KIT
Applicant
Dentimedic
Decision
Substantially Equivalent
Date received
1986-05-01
Decision date
1986-09-23
Days to decision
145 days
Clearance type
Traditional
Product code
EMB
Device class
1
Regulation number
872.3275
Medical specialty
Dental
Advisory committee
Dental
Location
Pocomoke City, MD, 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
Provicol QM Plus (K161630)Voco GmbH2016-09-15
DENTIST IN A BOX DENTAL EMERGENCY KIT PLUS TOOTH TRAUMA CARE KIT (K120695)Dentist IN A Box Pty., Ltd.2012-06-12
TEMPOCEM (K110759)Dmg USA, Inc.2011-06-10
PROVISA CEM (K073539)Cavex Holland BV2008-01-31
NON-EUGENOL TEMPORARY CEMENT (K020158)J. Morita USA, Inc.2002-03-07
DENTAL 911 (K941066)L.A.F. Industries, Inc.1995-05-24
EUGENOL USP (K862745)E&D Dental Manufacturing Co.1986-07-31
DEN TEMP (K821581)Majestic Drug Co., Inc.1982-06-14
OXYDENTAL ZINC OXIDE EUGENOL(ZOE)CEMENT (K801779)Oxy Dental Products, Inc.1980-08-07
KWIKAP (K772315)Den-Mat Corp.1978-01-03

Recalls involving this device

No recalls on record reference this clearance.