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FDA 510(k)

RRT SYSTEM LASER REFLECTOMETER ANALYZER

K-Number: K873407 · 1987-09-23

ApplicantIncstar Corp.
Decision Date1987-09-23
Product CodeJZW
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

RRT SYSTEM LASER REFLECTOMETER ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Incstar Corp.. It received FDA 510(k) clearance on 1987-09-23 under 510(k) number K873407. 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 RRT SYSTEM LASER REFLECTOMETER ANALYZER?

RRT SYSTEM LASER REFLECTOMETER ANALYZER is a medical device that received FDA 510(k) clearance on 1987-09-23. The listed applicant is Incstar Corp.. The 510(k) number is K873407.

When did RRT SYSTEM LASER REFLECTOMETER ANALYZER receive FDA 510(k) clearance?

RRT SYSTEM LASER REFLECTOMETER ANALYZER received FDA 510(k) clearance on 1987-09-23, under 510(k) number K873407.

Who is the listed applicant for RRT SYSTEM LASER REFLECTOMETER ANALYZER?

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

What is the FDA product code for RRT SYSTEM LASER REFLECTOMETER ANALYZER?

The FDA product code for RRT SYSTEM LASER REFLECTOMETER ANALYZER is JZW.

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Other records listing Incstar Corp. 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.

K963289INCSTAR TOXOPLASMA IGM CAPTURE ELISA ASSAYK963297INCSTAR TOXOPLASMA IGG FAST ELISA ASSAY (CAT.#7560)K963296INCSTAR TOXOPLASMA IGG ALISA ASSAY (CAT.#7565)K960367INCSTAR RUBELLA IGG ELISA ASSAYK960358INCSTAR RUBELLA IGG FAST ELISA ASSAYK960434INCSTAR CYTOMEGALOVIRUS IGM CAPTURE ELISA ASSAY MODEL 8530

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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.K761234BEHRING LASER NEPHELOMETERBehring Diagnostics, Inc.K892223BEHRING NEPHELOMETER 100Behring Diagnostics, Inc.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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