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FDA 510(k)

NEIS NZY

K-Number: K863216 · 1986-09-15

ApplicantCarr-Scarborough Microbiologicals, Inc.
Decision Date1986-09-15
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

NEIS NZY is the device name listed in this FDA 510(k) record. The listed applicant is Carr-Scarborough Microbiologicals, Inc.. It received FDA 510(k) clearance on 1986-09-15 under 510(k) number K863216. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEIS NZY?

NEIS NZY is a medical device that received FDA 510(k) clearance on 1986-09-15. The listed applicant is Carr-Scarborough Microbiologicals, Inc.. The 510(k) number is K863216.

When did NEIS NZY receive FDA 510(k) clearance?

NEIS NZY received FDA 510(k) clearance on 1986-09-15, under 510(k) number K863216.

Who is the listed applicant for NEIS NZY?

The FDA 510(k) record lists Carr-Scarborough Microbiologicals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEIS NZY?

The FDA product code for NEIS NZY is JTO.

Other records listing Carr-Scarborough Microbiologicals, Inc. as applicant

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Related Devices (Code: JTO)

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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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