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FDA 510(k)

JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS

K-Number: K873514 · 1987-09-24

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1987-09-24
Product CodeKWY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1987-09-24 under 510(k) number K873514. The device is classified under product code KWY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS?

JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS is a medical device that received FDA 510(k) clearance on 1987-09-24. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K873514.

When did JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS receive FDA 510(k) clearance?

JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS received FDA 510(k) clearance on 1987-09-24, under 510(k) number K873514.

Who is the listed applicant for JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS?

The FDA 510(k) record lists Johnson & Johnson Professionals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS?

The FDA product code for JOHNSON & JOHNSON BIPOLAR ENDOPROTHESIS is KWY.

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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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