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FDA 510(k)

LASERSHARE PRINT SPOOLER(2100[SOLARIS X86]/(1500[WINDOWS NT])

K-Number: K973422 · 1997-10-28

Decision Date1997-10-28
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LASERSHARE PRINT SPOOLER(2100[SOLARIS X86]/(1500[WINDOWS NT]) is the device name listed in this FDA 510(k) record. The listed applicant is Dejarnette Research Systems. It received FDA 510(k) clearance on 1997-10-28 under 510(k) number K973422. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASERSHARE PRINT SPOOLER(2100[SOLARIS X86]/(1500[WINDOWS NT])?

LASERSHARE PRINT SPOOLER(2100[SOLARIS X86]/(1500[WINDOWS NT]) is a medical device that received FDA 510(k) clearance on 1997-10-28. The listed applicant is Dejarnette Research Systems. The 510(k) number is K973422.

When did LASERSHARE PRINT SPOOLER(2100[SOLARIS X86]/(1500[WINDOWS NT]) receive FDA 510(k) clearance?

LASERSHARE PRINT SPOOLER(2100[SOLARIS X86]/(1500[WINDOWS NT]) received FDA 510(k) clearance on 1997-10-28, under 510(k) number K973422.

Who is the listed applicant for LASERSHARE PRINT SPOOLER(2100[SOLARIS X86]/(1500[WINDOWS NT])?

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

What is the FDA product code for LASERSHARE PRINT SPOOLER(2100[SOLARIS X86]/(1500[WINDOWS NT])?

The FDA product code for LASERSHARE PRINT SPOOLER(2100[SOLARIS X86]/(1500[WINDOWS NT]) is LMC.

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.

Other records listing Dejarnette Research Systems 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.

View all 9 devices →

Related Devices (Code: LMC)

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.

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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