STORZ MODEL M705 AND/OR M706 CEILING MOUNTED MICR.
K-Number: K903412 · 1990-09-20
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Device Summary
Frequently Asked Questions
What is the STORZ MODEL M705 AND/OR M706 CEILING MOUNTED MICR.?
STORZ MODEL M705 AND/OR M706 CEILING MOUNTED MICR. is a medical device that received FDA 510(k) clearance on 1990-09-20. The listed applicant is Storz Instrument Co.. The 510(k) number is K903412.
When did STORZ MODEL M705 AND/OR M706 CEILING MOUNTED MICR. receive FDA 510(k) clearance?
STORZ MODEL M705 AND/OR M706 CEILING MOUNTED MICR. received FDA 510(k) clearance on 1990-09-20, under 510(k) number K903412.
Who is the listed applicant for STORZ MODEL M705 AND/OR M706 CEILING MOUNTED MICR.?
The FDA 510(k) record lists Storz Instrument Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STORZ MODEL M705 AND/OR M706 CEILING MOUNTED MICR.?
The FDA product code for STORZ MODEL M705 AND/OR M706 CEILING MOUNTED MICR. is EPT.
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 Storz Instrument Co. 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: EPT)
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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