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FDA 510(k)

AUTOSPECT PLUS WITH INSTILL MOTION CORRECTION

K-Number: K992317 · 1999-10-01

ApplicantAdac Laboratories
Decision Date1999-10-01
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AUTOSPECT PLUS WITH INSTILL MOTION CORRECTION is the device name listed in this FDA 510(k) record. The listed applicant is Adac Laboratories. It received FDA 510(k) clearance on 1999-10-01 under 510(k) number K992317. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOSPECT PLUS WITH INSTILL MOTION CORRECTION?

AUTOSPECT PLUS WITH INSTILL MOTION CORRECTION is a medical device that received FDA 510(k) clearance on 1999-10-01. The listed applicant is Adac Laboratories. The 510(k) number is K992317.

When did AUTOSPECT PLUS WITH INSTILL MOTION CORRECTION receive FDA 510(k) clearance?

AUTOSPECT PLUS WITH INSTILL MOTION CORRECTION received FDA 510(k) clearance on 1999-10-01, under 510(k) number K992317.

Who is the listed applicant for AUTOSPECT PLUS WITH INSTILL MOTION CORRECTION?

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

What is the FDA product code for AUTOSPECT PLUS WITH INSTILL MOTION CORRECTION?

The FDA product code for AUTOSPECT PLUS WITH INSTILL MOTION CORRECTION is KPS.

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Other records listing Adac Laboratories 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.

K062298APOLLO GAMMA CAMERA SYSTEMK061029JETSTREAM WORKSPACEK060020AUTOQUANT PLUSK051351PRECEDENCE SPECT/CT IMAGING SYSTEMK042880JETSTREAM WORKSPACEK042903AUTOSPECS

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Related Devices (Code: KPS)

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.

K261305MICSI-PETMicrostructure Imaging, Inc.K261427uMI Panvivo (uMI Panvivo M)Shanghai United Imaging Healthcare Co., Ltd.K261315Symbia Pro.specta Q3 (11364751);Symbia Pro.specta X3 (11364752);Symbia Pro.specta X7 (11364753);Symbia Pro.specta VA40 FamilySiemens Medical Solutions USA, Inc.K260524uMI Panvivo (uMI Panvivo LS); uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES)Shanghai United Imaging Healthcare Co., Ltd.K253564uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES)Shanghai United Imaging Healthcare Co., Ltd.K254001VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464)Spectrum Dynamics Medical, Ltd.

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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