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FDA 510(k)

CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATT

K-Number: K926082 · 1992-12-30

ApplicantBiodan Medical Systems, Ltd.
Decision Date1992-12-30
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATT is the device name listed in this FDA 510(k) record. The listed applicant is Biodan Medical Systems, Ltd.. It received FDA 510(k) clearance on 1992-12-30 under 510(k) number K926082. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATT?

CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATT is a medical device that received FDA 510(k) clearance on 1992-12-30. The listed applicant is Biodan Medical Systems, Ltd.. The 510(k) number is K926082.

When did CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATT receive FDA 510(k) clearance?

CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATT received FDA 510(k) clearance on 1992-12-30, under 510(k) number K926082.

Who is the listed applicant for CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATT?

The FDA 510(k) record lists Biodan Medical Systems, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATT?

The FDA product code for CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATT is IZI.

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Other records listing Biodan Medical Systems, Ltd. 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.

K932153THYROID UPTAKE SYSTEM & ATOMLAB 950 MED. SPECTROMEK930261RTM REHABILITATION TREADMILL, MODEL #945-200K930262TREATMENT TABLE, MODEL #825-100K930259TRACTION TABLE MODEL #825-200K926083NUCLEAR PATIENT SANNING TABLES, VARIOUS TYPESK922591UROLOGICAL C-ARM TABLE, MODEL #056-450

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Related Devices (Code: IZI)

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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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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