MID-500
K-Number: K940117 · 1994-06-10
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Device Summary
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.
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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