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FDA 510(k)

BEHRING LASER NEPHELOMETER

K-Number: K761234 · 1990-06-07

ApplicantBehring Diagnostics, Inc.
Decision Date1990-06-07
Product CodeJZW
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

BEHRING LASER NEPHELOMETER 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 1990-06-07 under 510(k) number K761234. The device is classified under product code JZW. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEHRING LASER NEPHELOMETER?

BEHRING LASER NEPHELOMETER is a medical device that received FDA 510(k) clearance on 1990-06-07. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K761234.

When did BEHRING LASER NEPHELOMETER receive FDA 510(k) clearance?

BEHRING LASER NEPHELOMETER received FDA 510(k) clearance on 1990-06-07, under 510(k) number K761234.

Who is the listed applicant for BEHRING LASER NEPHELOMETER?

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 LASER NEPHELOMETER?

The FDA product code for BEHRING LASER NEPHELOMETER is JZW.

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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.

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Related Devices (Code: JZW)

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.

K001647BN PROSPEC SYSTEMDade Behring, Inc.K892223BEHRING NEPHELOMETER 100Behring Diagnostics, Inc.K873407RRT SYSTEM LASER REFLECTOMETER ANALYZERIncstar Corp.K873401TURBOXUnipath , Ltd.K801949BCM-302 COLLIMATING CONE & COMPENSATINB C Medical , Ltd.K801391DISC 120 TRANSPORTERTravenol Laboratories, S.A.

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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