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FDA 510(k)

NEVISCAN MODEL N - 100

K-Number: K884989 · 1989-02-28

ApplicantSpecial Products, Inc.
Decision Date1989-02-28
Product CodeHKI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NEVISCAN MODEL N - 100 is the device name listed in this FDA 510(k) record. The listed applicant is Special Products, Inc.. It received FDA 510(k) clearance on 1989-02-28 under 510(k) number K884989. The device is classified under product code HKI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEVISCAN MODEL N - 100?

NEVISCAN MODEL N - 100 is a medical device that received FDA 510(k) clearance on 1989-02-28. The listed applicant is Special Products, Inc.. The 510(k) number is K884989.

When did NEVISCAN MODEL N - 100 receive FDA 510(k) clearance?

NEVISCAN MODEL N - 100 received FDA 510(k) clearance on 1989-02-28, under 510(k) number K884989.

Who is the listed applicant for NEVISCAN MODEL N - 100?

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

What is the FDA product code for NEVISCAN MODEL N - 100?

The FDA product code for NEVISCAN MODEL N - 100 is HKI.

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Related Devices (Code: HKI)

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Official Source

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