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FDA 510(k)

LATEX R. TYPHI

K-Number: K860557 · 1986-04-21

ApplicantHealth Research, Inc.
Decision Date1986-04-21
Product CodeGPM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LATEX R. TYPHI 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 1986-04-21 under 510(k) number K860557. The device is classified under product code GPM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LATEX R. TYPHI?

LATEX R. TYPHI is a medical device that received FDA 510(k) clearance on 1986-04-21. The listed applicant is Health Research, Inc.. The 510(k) number is K860557.

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

LATEX R. TYPHI received FDA 510(k) clearance on 1986-04-21, under 510(k) number K860557.

Who is the listed applicant for LATEX R. TYPHI?

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. TYPHI?

The FDA product code for LATEX R. TYPHI is GPM.

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.

K872129LATEX R. CONORIIK843794LATEX-R RICKETTSII

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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