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FDA 510(k)

BEHRING RAPIGNOST TOTAL SCREEN L URINE TEST STRIPS

K-Number: K861255 · 1986-10-03

Decision Date1986-10-03
Product CodeJIL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BEHRING RAPIGNOST TOTAL SCREEN L URINE TEST STRIPS is the device name listed in this FDA 510(k) record. The listed applicant is Behring Diagnostics, Inc.. It received FDA 510(k) clearance on 1986-10-03 under 510(k) number K861255. The device is classified under product code JIL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEHRING RAPIGNOST TOTAL SCREEN L URINE TEST STRIPS?

BEHRING RAPIGNOST TOTAL SCREEN L URINE TEST STRIPS is a medical device that received FDA 510(k) clearance on 1986-10-03. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K861255.

When did BEHRING RAPIGNOST TOTAL SCREEN L URINE TEST STRIPS receive FDA 510(k) clearance?

BEHRING RAPIGNOST TOTAL SCREEN L URINE TEST STRIPS received FDA 510(k) clearance on 1986-10-03, under 510(k) number K861255.

Who is the listed applicant for BEHRING RAPIGNOST TOTAL SCREEN L URINE TEST STRIPS?

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

What is the FDA product code for BEHRING RAPIGNOST TOTAL SCREEN L URINE TEST STRIPS?

The FDA product code for BEHRING RAPIGNOST TOTAL SCREEN L URINE TEST STRIPS is JIL.

Related Clinical Trials

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.

Other records listing Behring Diagnostics, Inc. as applicant

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.

View all 145 devices →

Related Devices (Code: JIL)

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.

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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