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FDA 510(k)

IMATRON C-100 ULTRAFAST CT SCANNER

K-Number: K872615 · 1987-09-23

ApplicantImatron, Inc.
Decision Date1987-09-23
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMATRON C-100 ULTRAFAST CT SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Imatron, Inc.. It received FDA 510(k) clearance on 1987-09-23 under 510(k) number K872615. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMATRON C-100 ULTRAFAST CT SCANNER?

IMATRON C-100 ULTRAFAST CT SCANNER is a medical device that received FDA 510(k) clearance on 1987-09-23. The listed applicant is Imatron, Inc.. The 510(k) number is K872615.

When did IMATRON C-100 ULTRAFAST CT SCANNER receive FDA 510(k) clearance?

IMATRON C-100 ULTRAFAST CT SCANNER received FDA 510(k) clearance on 1987-09-23, under 510(k) number K872615.

Who is the listed applicant for IMATRON C-100 ULTRAFAST CT SCANNER?

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

What is the FDA product code for IMATRON C-100 ULTRAFAST CT SCANNER?

The FDA product code for IMATRON C-100 ULTRAFAST CT SCANNER is JAK.

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 Imatron, 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.

View all 11 devices →

Related Devices (Code: JAK)

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

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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