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FDA 510(k)

JOHNSON & JOHNSON AUSTIN MOORE STEM

K-Number: K955385 · 1996-01-30

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1996-01-30
Product CodeKWL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

JOHNSON & JOHNSON AUSTIN MOORE STEM 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 1996-01-30 under 510(k) number K955385. The device is classified under product code KWL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOHNSON & JOHNSON AUSTIN MOORE STEM?

JOHNSON & JOHNSON AUSTIN MOORE STEM is a medical device that received FDA 510(k) clearance on 1996-01-30. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K955385.

When did JOHNSON & JOHNSON AUSTIN MOORE STEM receive FDA 510(k) clearance?

JOHNSON & JOHNSON AUSTIN MOORE STEM received FDA 510(k) clearance on 1996-01-30, under 510(k) number K955385.

Who is the listed applicant for JOHNSON & JOHNSON AUSTIN MOORE STEM?

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 AUSTIN MOORE STEM?

The FDA product code for JOHNSON & JOHNSON AUSTIN MOORE STEM is KWL.

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Other records listing Johnson & Johnson Professionals, Inc. as applicant

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Related Devices (Code: KWL)

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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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