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FDA 510(k)

CTAPI - NEISSERA SCREEN

K-Number: K850982 · 1985-03-29

ApplicantAnalytical Products, Inc.
Decision Date1985-03-29
Product CodeJSE
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CTAPI - NEISSERA SCREEN is the device name listed in this FDA 510(k) record. The listed applicant is Analytical Products, Inc.. It received FDA 510(k) clearance on 1985-03-29 under 510(k) number K850982. The device is classified under product code JSE. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CTAPI - NEISSERA SCREEN?

CTAPI - NEISSERA SCREEN is a medical device that received FDA 510(k) clearance on 1985-03-29. The listed applicant is Analytical Products, Inc.. The 510(k) number is K850982.

When did CTAPI - NEISSERA SCREEN receive FDA 510(k) clearance?

CTAPI - NEISSERA SCREEN received FDA 510(k) clearance on 1985-03-29, under 510(k) number K850982.

Who is the listed applicant for CTAPI - NEISSERA SCREEN?

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

What is the FDA product code for CTAPI - NEISSERA SCREEN?

The FDA product code for CTAPI - NEISSERA SCREEN is JSE.

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Other records listing Analytical Products, Inc. as applicant

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Related Devices (Code: JSE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K962265MLX MICROTITER PLATE LUMINOMETERDynatech Laboratories, Inc.K883995X-ACT UREA/TDAPro-Lab, Inc.K883996X-ACT LDC/INDPro-Lab, Inc.K880133MIL MEDIUMHardy MediaK880116MRVP BROTHHardy MediaK874537KLIGLER IRON AGAR AND TRIPLE SUGAR IRON AGARLakewood Biochemical Co., Inc.

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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