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FDA 510(k)

TREATMENT TABLE, MODEL #825-100

K-Number: K930262 · 1993-03-29

Decision Date1993-03-29
Product CodeINO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TREATMENT TABLE, MODEL #825-100 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 1993-03-29 under 510(k) number K930262. The device is classified under product code INO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TREATMENT TABLE, MODEL #825-100?

TREATMENT TABLE, MODEL #825-100 is a medical device that received FDA 510(k) clearance on 1993-03-29. The listed applicant is Biodan Medical Systems, Ltd.. The 510(k) number is K930262.

When did TREATMENT TABLE, MODEL #825-100 receive FDA 510(k) clearance?

TREATMENT TABLE, MODEL #825-100 received FDA 510(k) clearance on 1993-03-29, under 510(k) number K930262.

Who is the listed applicant for TREATMENT TABLE, MODEL #825-100?

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 TREATMENT TABLE, MODEL #825-100?

The FDA product code for TREATMENT TABLE, MODEL #825-100 is INO.

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 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.

View all 20 devices →

Related Devices (Code: INO)

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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