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FDA 510(k)

E-TYPE SPEED REDUCER CONTRA ANGLE

K-Number: K970953 · 1997-04-15

ApplicantNsk Nakanishi, Inc.
Decision Date1997-04-15
Product CodeKMW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

E-TYPE SPEED REDUCER CONTRA ANGLE is the device name listed in this FDA 510(k) record. The listed applicant is Nsk Nakanishi, Inc.. It received FDA 510(k) clearance on 1997-04-15 under 510(k) number K970953. The device is classified under product code KMW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E-TYPE SPEED REDUCER CONTRA ANGLE?

E-TYPE SPEED REDUCER CONTRA ANGLE is a medical device that received FDA 510(k) clearance on 1997-04-15. The listed applicant is Nsk Nakanishi, Inc.. The 510(k) number is K970953.

When did E-TYPE SPEED REDUCER CONTRA ANGLE receive FDA 510(k) clearance?

E-TYPE SPEED REDUCER CONTRA ANGLE received FDA 510(k) clearance on 1997-04-15, under 510(k) number K970953.

Who is the listed applicant for E-TYPE SPEED REDUCER CONTRA ANGLE?

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

What is the FDA product code for E-TYPE SPEED REDUCER CONTRA ANGLE?

The FDA product code for E-TYPE SPEED REDUCER CONTRA ANGLE is KMW.

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Other records listing Nsk Nakanishi, Inc. as applicant

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Related Devices (Code: KMW)

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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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