Atlas FDA

FLORIDA PROBE

FDA 510(k) clearance K875076 · decided 1988-03-10

Clearance details

K-number
K875076
Device name
FLORIDA PROBE
Applicant
Florida Probe Corp.
Decision
Substantially Equivalent
Date received
1987-12-09
Decision date
1988-03-10
Days to decision
92 days
Clearance type
Traditional
Product code
EIX
Device class
1
Regulation number
872.4565
Medical specialty
Dental
Advisory committee
Dental
Location
Gainesville, 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
VIP VICTOR INTERACTIVE PROBE (K960245)Pro-Dentec1996-04-04
THE VIVACARE T.P.S. PROBE (K944848)Rms Div.1994-12-14
PROBE TIP/PERI PROBE/PERI PROBE COMP. (K936221)Pd International AB1994-08-01
ALBUMIN REAGENT (K890333)Alpkem Corp.1989-02-17
ACCUTEK PERIODONTAL PROBE (K880827)Sweet Micro Systems, Inc.1988-04-12
ACCUDENT ACCUPROBE (K870280)Accudent, Inc.1987-06-08
DISPOSABLE PERIODONTAL PROBE (K871504)Periodontal Health Brush, Inc.1987-05-06
DENTAL INSTRUMENTS - PROBES (K823324)Miltex, Inc.1982-11-24

Recalls involving this device

No recalls on record reference this clearance.