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FDA 510(k)

TANGENT II

K-Number: K883974 · 1988-10-20

ApplicantFischer Imaging Corp.
Decision Date1988-10-20
Product CodeIZZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TANGENT II is the device name listed in this FDA 510(k) record. The listed applicant is Fischer Imaging Corp.. It received FDA 510(k) clearance on 1988-10-20 under 510(k) number K883974. The device is classified under product code IZZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TANGENT II?

TANGENT II is a medical device that received FDA 510(k) clearance on 1988-10-20. The listed applicant is Fischer Imaging Corp.. The 510(k) number is K883974.

When did TANGENT II receive FDA 510(k) clearance?

TANGENT II received FDA 510(k) clearance on 1988-10-20, under 510(k) number K883974.

Who is the listed applicant for TANGENT II?

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

What is the FDA product code for TANGENT II?

The FDA product code for TANGENT II is IZZ.

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Other records listing Fischer Imaging Corp. 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.

K042095MAMMOTESTK021113MAMMOPATHK981414LC POSITIONERK973400MAMMOTEST ADAPTER DRIVERK964806MD-1835K961207EP-X BIPLANE

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Related Devices (Code: IZZ)

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.

K971452MULTIX TOP/PRO RADIOGRAPHIC X-RAY TABLESiemens Medical Solutions USA, Inc.K952701MED-TRON SPECT IMAGING TABLEMed-Tron Products, Inc.K951315CATHETERIZATION TABLE KS-60Shimadzu Medical SystemsK951053ANGIOREX CAT-350BToshiba America Medical Systems, In.CK943926RAPIDO 2000 AUTOMATIC RADIOGRAPHIC TABLEPhilips Medical Systems (Cleveland), Inc.K930273ALPHARaymax Medical Corp.

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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