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FDA 510(k)

NORELCO VIBRATING BOARD V900

K-Number: K830715 · 1983-05-25

ApplicantNorth American Philips Corp.
Decision Date1983-05-25
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NORELCO VIBRATING BOARD V900 is the device name listed in this FDA 510(k) record. The listed applicant is North American Philips Corp.. It received FDA 510(k) clearance on 1983-05-25 under 510(k) number K830715. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORELCO VIBRATING BOARD V900?

NORELCO VIBRATING BOARD V900 is a medical device that received FDA 510(k) clearance on 1983-05-25. The listed applicant is North American Philips Corp.. The 510(k) number is K830715.

When did NORELCO VIBRATING BOARD V900 receive FDA 510(k) clearance?

NORELCO VIBRATING BOARD V900 received FDA 510(k) clearance on 1983-05-25, under 510(k) number K830715.

Who is the listed applicant for NORELCO VIBRATING BOARD V900?

The FDA 510(k) record lists North American Philips Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NORELCO VIBRATING BOARD V900?

The FDA product code for NORELCO VIBRATING BOARD V900 is IRO.

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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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