Fastray LC

FDA 510(k) K991631 · Harry J. Bosworth Co.

Substantially Equivalent

510(k) numberK991631

Submission

Device name
Fastray LC
Applicant
Harry J. Bosworth Co.
Skokie, IL, US
Received
May 11, 1999
Decision date
July 26, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
ELW – Material, Impression
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3660
Specialty
Dental

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Questions and answers

When was Fastray LC cleared by the FDA?

Fastray LC (K991631) received a 510(k) decision of Substantially Equivalent on July 26, 1999, 76 days after the submission was received.

What is the product code of K991631?

The FDA product code is ELW – Material, Impression, a Class II (moderate risk) device regulated under 21 CFR 872.3660.