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FDA 510(k)

SEQUENTIAL SAMPLE MULTI-PHOTON DETECTOR

K-Number: K962762 · 1996-08-16

ApplicantBiotraces, Inc.
Decision Date1996-08-16
Product CodeJJJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SEQUENTIAL SAMPLE MULTI-PHOTON DETECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Biotraces, Inc.. It received FDA 510(k) clearance on 1996-08-16 under 510(k) number K962762. The device is classified under product code JJJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEQUENTIAL SAMPLE MULTI-PHOTON DETECTOR?

SEQUENTIAL SAMPLE MULTI-PHOTON DETECTOR is a medical device that received FDA 510(k) clearance on 1996-08-16. The listed applicant is Biotraces, Inc.. The 510(k) number is K962762.

When did SEQUENTIAL SAMPLE MULTI-PHOTON DETECTOR receive FDA 510(k) clearance?

SEQUENTIAL SAMPLE MULTI-PHOTON DETECTOR received FDA 510(k) clearance on 1996-08-16, under 510(k) number K962762.

Who is the listed applicant for SEQUENTIAL SAMPLE MULTI-PHOTON DETECTOR?

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

What is the FDA product code for SEQUENTIAL SAMPLE MULTI-PHOTON DETECTOR?

The FDA product code for SEQUENTIAL SAMPLE MULTI-PHOTON DETECTOR is JJJ.

Related Clinical Trials

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: JJJ)

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.

K946387CAPRA (CAPRAC-R) WIPETEST AND WELL COUNTERCapintec, Inc.K920559ABBOTT VERTEX ANALYZERAbbott LaboratoriesK900087GENESYS 6000 GAMMA COUNTERLaboratory Technologies, Inc.K896202MATRIX(TM)-96Canberra Industries, Inc.K894902SOURCEREROakfield Instruments, Ltd.K884091SOURCERERJohn Caunt Scientific , Ltd.

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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