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FDA 510(k)

EAR PIERCING DEVICE

K-Number: K772171 · 1978-01-03

ApplicantRobert C. Cameron
Decision Date1978-01-03
Product CodeJYS
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EAR PIERCING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Robert C. Cameron. It received FDA 510(k) clearance on 1978-01-03 under 510(k) number K772171. The device is classified under product code JYS. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAR PIERCING DEVICE?

EAR PIERCING DEVICE is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Robert C. Cameron. The 510(k) number is K772171.

When did EAR PIERCING DEVICE receive FDA 510(k) clearance?

EAR PIERCING DEVICE received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772171.

Who is the listed applicant for EAR PIERCING DEVICE?

The FDA 510(k) record lists Robert C. Cameron as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EAR PIERCING DEVICE?

The FDA product code for EAR PIERCING DEVICE is JYS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: JYS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K860622STUDEX EAR PIERCING GUNSOnyx Industries, Inc.K860678J.K. TEMPLETON EAR PIERCING GUNS/INSTRUMENTS/STUDSJay Kenny Templeton

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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