Beach Surgical Pliers Non-Hook

FDA 510(k) K821787 · Pacific Dental Corp.

Substantially Equivalent

510(k) numberK821787

Submission

Device name
Beach Surgical Pliers Non-Hook
Applicant
Pacific Dental Corp.
Mchenry, IL, US
Received
June 17, 1982
Decision date
July 6, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EJY – Pliers, Operative
Device class
Class I (low risk)
Regulation
21 CFR 872.4565
Specialty
Dental

Other 510(k)s with product code EJY

510(k)DeviceApplicantDecision
K8517302710 to 2935 Various Pliers for Orthodontics/ProstEJY · Traditional Artiberia07/02/1985SE

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Questions and answers

When was Beach Surgical Pliers Non-Hook cleared by the FDA?

Beach Surgical Pliers Non-Hook (K821787) received a 510(k) decision of Substantially Equivalent on July 6, 1982, 19 days after the submission was received.

What is the product code of K821787?

The FDA product code is EJY – Pliers, Operative, a Class I (low risk) device regulated under 21 CFR 872.4565.