FDA 510(k)

NRBC-CHEX FOR LH

K-Number: K060083 · 2006-02-09

ApplicantStreck

Decision Date2006-02-09

Product CodeGJR

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

NRBC-CHEX FOR LH is the device name listed in this FDA 510(k) record. The listed applicant is Streck. It received FDA 510(k) clearance on 2006-02-09 under 510(k) number K060083. The device is classified under product code GJR. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NRBC-CHEX FOR LH?

NRBC-CHEX FOR LH is a medical device that received FDA 510(k) clearance on 2006-02-09. The listed applicant is Streck. The 510(k) number is K060083.

When did NRBC-CHEX FOR LH receive FDA 510(k) clearance?

NRBC-CHEX FOR LH received FDA 510(k) clearance on 2006-02-09, under 510(k) number K060083.

Who is the listed applicant for NRBC-CHEX FOR LH?

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

What is the FDA product code for NRBC-CHEX FOR LH?

The FDA product code for NRBC-CHEX FOR LH is GJR.

Other records listing Streck 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.

K254166MDx-Chex for BCN K231221MDx-Chex for BC-GP K231223MDx-Chex for BC-GN K170091UA-Cellular Complete K160585XN CAL K160590XN CHECK

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Related Devices (Code: GJR)

K080016NRBC-CHEX FOR ADVIAStreck K000076CELL-CHEXStreck Laboratories, Inc.K940430SEDRATROLMedical Specialties Intl., Inc.K900484RET-CHECKStreck Laboratories, 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.