Atlas FDA

NITE-GUIDE

FDA 510(k) clearance K931615 · decided 1995-04-14

Clearance details

K-number
K931615
Device name
NITE-GUIDE
Applicant
ORTHO-TAIN, Inc.
Decision
Substantially Equivalent
Date received
1993-04-01
Decision date
1995-04-14
Days to decision
743 days
Clearance type
Traditional
Product code
KMY
Device class
1
Regulation number
872.5525
Medical specialty
Dental
Advisory committee
Dental
Location
Chicago, 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
DENT-O-CRYL ORTHODONTIC ACRYLIC (K942667)Dentauraum, Inc.1995-02-13
GLENROE ELASTIBITE STIMULATOR (K924351)Glenroe Technologies1994-01-06
RELAX-O-GUARD (K925064)Aquatemp Service Co., Inc.1993-09-13
THE ORTHOTRAINER (K924975)Myofunctional Research Corp. Pty. , Ltd.1993-07-08
THE TMJ APPLIANCE (K924974)Myofunctional Research Corp. Pty. , Ltd.1993-06-23
PERFORMED TEMPLATE W/FRAGRANCE FOR TOOTH POSTIONER (K904128)American Orthodontics1990-11-09
PREFORMED TEMPLATE FOR TOOTH POSITIONER (K891328)American Orthodontics1989-03-31
REMOLDABLE CRANIOMANDIBULAR APPLIANCE (K833455)Jeffrey H. Attlin1984-01-10
AQUALIZER MOUTHPIECE (K831793)Martin D. Lerman1983-08-12
DYNAMIC FUNTIONAL POSITIONER (K821458)Dynamic Functional Positioner, Inc.1982-06-09
PREFORMED TOOTH POSITIONER (K780619)Tp Laboratories, Inc.1978-06-28

Recalls involving this device

No recalls on record reference this clearance.