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FDA 510(k)

LD2000 SERIES

K-Number: K980565 · 1998-03-19

ApplicantGeneral Scanning, Inc.
Decision Date1998-03-19
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LD2000 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is General Scanning, Inc.. It received FDA 510(k) clearance on 1998-03-19 under 510(k) number K980565. The device is classified under product code LMA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LD2000 SERIES?

LD2000 SERIES is a medical device that received FDA 510(k) clearance on 1998-03-19. The listed applicant is General Scanning, Inc.. The 510(k) number is K980565.

When did LD2000 SERIES receive FDA 510(k) clearance?

LD2000 SERIES received FDA 510(k) clearance on 1998-03-19, under 510(k) number K980565.

Who is the listed applicant for LD2000 SERIES?

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

What is the FDA product code for LD2000 SERIES?

The FDA product code for LD2000 SERIES is LMA.

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Other records listing General Scanning, 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.

K973411DIGMI-2000 (GSI INTERNAL REFERENCE)/LD2800 (MARKETING NAME)K923536NUCLEAR MEDICINE LASER IMAGER

Related Devices (Code: LMA)

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.

K132183DICOM VIDEOBar Code Computer, Ltd.K130636TELERADPRO EDGE; TELERADPRO EDGE HD-CCDVidar Systems Corp.K130406DIAGNOSTICPRO EDGEVidar Systems Corp.K102476TELERADPROVidar Systems Corp.K093809VIDAR DENTAL FILM DIGITIZERVidar Systems Corp.K091288MEDI-6000 MEDICAL IMAGE DIGITIZERMicrotek International, Inc.

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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