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FDA 510(k)

SERVO MED NYSTAGMOGRAPH NG-1

K-Number: K843004 · 1984-10-30

ApplicantServo Med, Inc.
Decision Date1984-10-30
Product CodeGWN
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SERVO MED NYSTAGMOGRAPH NG-1 is the device name listed in this FDA 510(k) record. The listed applicant is Servo Med, Inc.. It received FDA 510(k) clearance on 1984-10-30 under 510(k) number K843004. The device is classified under product code GWN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERVO MED NYSTAGMOGRAPH NG-1?

SERVO MED NYSTAGMOGRAPH NG-1 is a medical device that received FDA 510(k) clearance on 1984-10-30. The listed applicant is Servo Med, Inc.. The 510(k) number is K843004.

When did SERVO MED NYSTAGMOGRAPH NG-1 receive FDA 510(k) clearance?

SERVO MED NYSTAGMOGRAPH NG-1 received FDA 510(k) clearance on 1984-10-30, under 510(k) number K843004.

Who is the listed applicant for SERVO MED NYSTAGMOGRAPH NG-1?

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

What is the FDA product code for SERVO MED NYSTAGMOGRAPH NG-1?

The FDA product code for SERVO MED NYSTAGMOGRAPH NG-1 is GWN.

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Official Source

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

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