Atlas FDA

PULPTESTER MODEL 2001

FDA 510(k) clearance K790799 · decided 1979-05-31

Clearance details

K-number
K790799
Device name
PULPTESTER MODEL 2001
Applicant
Analytic Technology
Decision
Substantially Equivalent
Date received
1979-04-24
Decision date
1979-05-31
Days to decision
37 days
Clearance type
Traditional
Product code
EAT
Device class
2
Regulation number
872.1720
Medical specialty
Dental
Advisory committee
Dental
Location
Mchenry, IL, 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
THERMIQUE (K022097)Parkell, Inc.2002-09-06
ELEMENTS DIAGNOSTIC UNIT (K021298)Sybron Endo/Analytic2002-06-19
PHARMAETHYL LOCAL PULP AND VITALITY TESTING AGENT (K012427)Specialites Septodont2001-10-09
CHILLIT (K011666)Heatshield, Inc.2001-08-06
ENDO ANALYZER, MODEL 8005, MODIFIED (K990225)Sybron Dental Specialties, Inc.1999-02-25
ENDO ANALYZER, MODEL 8005 (K973439)Sybron Dental Specialties, Inc.1997-12-08
SYSTEM B HEAT SOURCE (K970715)Sybron Dental Specialties, Inc.1997-04-07
TOUCH N' HEAT (K963862)Sybron Dental Specialties, Inc.1996-12-02
ORTHO-ICE (K960799)Ultimate Wireforms, Inc.1996-05-09
DIGITEST (K950237)Parkell, Inc.1995-06-09
GENTAL PULSE (K950238)Parkell, Inc.1995-05-09
THERMAL PULP TESTER (K940260)Union Broach, Div. Moyco Industries, Inc.1994-03-07

Recalls involving this device

No recalls on record reference this clearance.