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FDA 510(k)

LATEX R. CONORII

K-Number: K872129 · 1987-08-19

ApplicantHealth Research, Inc.
Decision Date1987-08-19
Product CodeLSQ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LATEX R. CONORII is the device name listed in this FDA 510(k) record. The listed applicant is Health Research, Inc.. It received FDA 510(k) clearance on 1987-08-19 under 510(k) number K872129. The device is classified under product code LSQ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LATEX R. CONORII?

LATEX R. CONORII is a medical device that received FDA 510(k) clearance on 1987-08-19. The listed applicant is Health Research, Inc.. The 510(k) number is K872129.

When did LATEX R. CONORII receive FDA 510(k) clearance?

LATEX R. CONORII received FDA 510(k) clearance on 1987-08-19, under 510(k) number K872129.

Who is the listed applicant for LATEX R. CONORII?

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

What is the FDA product code for LATEX R. CONORII?

The FDA product code for LATEX R. CONORII is LSQ.

Related Clinical Trials

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Other records listing Health Research, 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.

K860557LATEX R. TYPHIK843794LATEX-R RICKETTSII

Related Devices (Code: LSQ)

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.

K971591INDX DIP-S-TICKS SCRUB TYPHUS TEST FOR THE DETECTION OF IGG AND IGM ANTIBODIES TO ORIENTIA TSUTSUGAMUSHI (SCRUB TYPHUS)David C. Bishop, Ph.D.K920569INDXTM DIP-S-TICKSTMIntercare Diagnostics, Inc.K901597INDX DIP S TICKSIntercare Diagnostics, Inc.

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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