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FDA 510(k)

LONGPORT MODEL LDS -1

K-Number: K990238 · 1999-06-23

ApplicantLongport, Inc.
Decision Date1999-06-23
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LONGPORT MODEL LDS -1 is the device name listed in this FDA 510(k) record. The listed applicant is Longport, Inc.. It received FDA 510(k) clearance on 1999-06-23 under 510(k) number K990238. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LONGPORT MODEL LDS -1?

LONGPORT MODEL LDS -1 is a medical device that received FDA 510(k) clearance on 1999-06-23. The listed applicant is Longport, Inc.. The 510(k) number is K990238.

When did LONGPORT MODEL LDS -1 receive FDA 510(k) clearance?

LONGPORT MODEL LDS -1 received FDA 510(k) clearance on 1999-06-23, under 510(k) number K990238.

Who is the listed applicant for LONGPORT MODEL LDS -1?

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

What is the FDA product code for LONGPORT MODEL LDS -1?

The FDA product code for LONGPORT MODEL LDS -1 is IYO.

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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Other records listing Longport, 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.

K062571LONGPORT EPISCAN, MODEL-I-200

Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, 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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