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FDA 510(k)

GRASEBY ANDERSEN'S, INTEGRITY S700

K-Number: K963131 · 1997-02-14

ApplicantGraseby Andersen
Decision Date1997-02-14
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GRASEBY ANDERSEN'S, INTEGRITY S700 is the device name listed in this FDA 510(k) record. The listed applicant is Graseby Andersen. It received FDA 510(k) clearance on 1997-02-14 under 510(k) number K963131. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRASEBY ANDERSEN'S, INTEGRITY S700?

GRASEBY ANDERSEN'S, INTEGRITY S700 is a medical device that received FDA 510(k) clearance on 1997-02-14. The listed applicant is Graseby Andersen. The 510(k) number is K963131.

When did GRASEBY ANDERSEN'S, INTEGRITY S700 receive FDA 510(k) clearance?

GRASEBY ANDERSEN'S, INTEGRITY S700 received FDA 510(k) clearance on 1997-02-14, under 510(k) number K963131.

Who is the listed applicant for GRASEBY ANDERSEN'S, INTEGRITY S700?

The FDA 510(k) record lists Graseby Andersen as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRASEBY ANDERSEN'S, INTEGRITY S700?

The FDA product code for GRASEBY ANDERSEN'S, INTEGRITY S700 is BZG.

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Official Source

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