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FDA 510(k)

TRACTION TABLE MODEL #825-200

K-Number: K930259 · 1993-03-24

ApplicantBiodan Medical Systems, Ltd.
Decision Date1993-03-24
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRACTION TABLE MODEL #825-200 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 1993-03-24 under 510(k) number K930259. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRACTION TABLE MODEL #825-200?

TRACTION TABLE MODEL #825-200 is a medical device that received FDA 510(k) clearance on 1993-03-24. The listed applicant is Biodan Medical Systems, Ltd.. The 510(k) number is K930259.

When did TRACTION TABLE MODEL #825-200 receive FDA 510(k) clearance?

TRACTION TABLE MODEL #825-200 received FDA 510(k) clearance on 1993-03-24, under 510(k) number K930259.

Who is the listed applicant for TRACTION TABLE MODEL #825-200?

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 TRACTION TABLE MODEL #825-200?

The FDA product code for TRACTION TABLE MODEL #825-200 is JFB.

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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 #825-100K926083NUCLEAR PATIENT SANNING TABLES, VARIOUS TYPESK926082CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATTK922591UROLOGICAL C-ARM TABLE, MODEL #056-450

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Related Devices (Code: JFB)

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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