Davis Lead Apron Gonadal Shield-Various Cat. Nos.

FDA 510(k) K912327 · Davis Lead Aprons, Inc.

Substantially Equivalent

510(k) numberK912327

Submission

Device name
Davis Lead Apron Gonadal Shield-Various Cat. Nos.
Applicant
Davis Lead Aprons, Inc.
Houston, TX, US
Received
May 24, 1991
Decision date
March 18, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KPY – Shield, Protective, Personnel
Device class
Class I (low risk)
Regulation
21 CFR 892.6500
Specialty
Radiology

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K934206Mavig Angio Shield Models 6290 & 6272KPY · Traditional F. Walter Hanel GmbH10/07/1993SE
K912378Davis Lead Apron/Radiographic Various Cat. NumbersKPY · Traditional Davis Lead Aprons, Inc.03/18/1992SE

More from Davis Lead Aprons, Inc.

510(k)DeviceDecision
K912378Davis Lead Apron/Radiographic Various Cat. NumbersKPY · Traditional 03/18/1992SE
K912326Davis Lead Apron - Various Catalogue NumbersKPY · Traditional 03/18/1992SE

Questions and answers

When was Davis Lead Apron Gonadal Shield-Various Cat. Nos. cleared by the FDA?

Davis Lead Apron Gonadal Shield-Various Cat. Nos. (K912327) received a 510(k) decision of Substantially Equivalent on March 18, 1992, 299 days after the submission was received.

What is the product code of K912327?

The FDA product code is KPY – Shield, Protective, Personnel, a Class I (low risk) device regulated under 21 CFR 892.6500.