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FDA 510(k)

TOMOMATIC 232

K-Number: K862511 · 1987-07-10

ApplicantMedimatic
Decision Date1987-07-10
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TOMOMATIC 232 is the device name listed in this FDA 510(k) record. The listed applicant is Medimatic. It received FDA 510(k) clearance on 1987-07-10 under 510(k) number K862511. 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 TOMOMATIC 232?

TOMOMATIC 232 is a medical device that received FDA 510(k) clearance on 1987-07-10. The listed applicant is Medimatic. The 510(k) number is K862511.

When did TOMOMATIC 232 receive FDA 510(k) clearance?

TOMOMATIC 232 received FDA 510(k) clearance on 1987-07-10, under 510(k) number K862511.

Who is the listed applicant for TOMOMATIC 232?

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

What is the FDA product code for TOMOMATIC 232?

The FDA product code for TOMOMATIC 232 is KPS.

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 Medimatic 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.

K851128DIGITMATIC DM2K810006TOMOMATIC 64K781742INHAMATIC 33K781352STRAIN GAUGE PLETHYSMOGRAPH

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

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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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