Atlas FDA

LIGHT, INSIDE

FDA 510(k) clearance K781878 · decided 1978-12-29

Clearance details

K-number
K781878
Device name
LIGHT, INSIDE
Applicant
Midwest
Decision
Substantially Equivalent
Date received
1978-11-06
Decision date
1978-12-29
Days to decision
53 days
Clearance type
Traditional
Product code
EAY
Device class
1
Regulation number
872.4620
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
MODEL A15-101 (K953191)Beaverstate Dental, Inc.1995-09-05
MODEL A15-103 (K953192)Beaverstate Dental, Inc.1995-09-05
JEDENTAL VLC DENTAL CURING LIGHT (K935718)Jedental Co., Inc.1994-01-26
STRYKERSCOPE TM/ORTHOSCOPE TM/STRYKER MINISCOPE TM (K871816)Stryker Corp.1987-08-03
POWER OPTIC (K831976)Ritter Co.1983-08-12
DENTAL ELECTRONIC/S.B.R TRADING BU HAND (K831824)Silverman'S1983-08-11
DENTISCOPE (K820907)Chayes Virginia, Inc.1982-05-05
FIBER OPTIC LIGHT SOURCE I (K812605)Venture Technology, Inc.1981-10-02
HELIOMAT (K802684)Vivadent (Usa), Inc.1980-11-24
DEN-MAT FIBER OPTIC HALOGEN LIGHT (K802716)Den-Mat Corp.1980-11-12
FIBER OPTIC HOSE (K801592)Lares Manufacturing Co., Inc.1980-07-21
FIBER OPTIC ILLUMINATOR (K801591)Lares Manufacturing Co., Inc.1980-07-21

Recalls involving this device

No recalls on record reference this clearance.