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FDA 510(k)

MID-500

K-Number: K940117 · 1994-06-10

Decision Date1994-06-10
Product CodeMEB
Advisory CommitteeHO
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

MID-500 is the device name listed in this FDA 510(k) record. The listed applicant is Block Medical, Inc.. It received FDA 510(k) clearance on 1994-06-10 under 510(k) number K940117. The device is classified under product code MEB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the MID-500?

MID-500 is a medical device that received FDA 510(k) clearance on 1994-06-10. The listed applicant is Block Medical, Inc.. The 510(k) number is K940117.

When did MID-500 receive FDA 510(k) clearance?

MID-500 received FDA 510(k) clearance on 1994-06-10, under 510(k) number K940117.

Who is the listed applicant for MID-500?

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

What is the FDA product code for MID-500?

The FDA product code for MID-500 is MEB.

Other records listing Block Medical, 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 12 devices →

Related Devices (Code: MEB)

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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