MODEL H 607-.67M2 30 MICRON RP AN69 MEM
K-Number: K800536 · 1980-08-07
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Device Summary
Frequently Asked Questions
What is the MODEL H 607-.67M2 30 MICRON RP AN69 MEM?
MODEL H 607-.67M2 30 MICRON RP AN69 MEM is a medical device that received FDA 510(k) clearance on 1980-08-07. The listed applicant is Hospal Medical Corp.. The 510(k) number is K800536.
When did MODEL H 607-.67M2 30 MICRON RP AN69 MEM receive FDA 510(k) clearance?
MODEL H 607-.67M2 30 MICRON RP AN69 MEM received FDA 510(k) clearance on 1980-08-07, under 510(k) number K800536.
Who is the listed applicant for MODEL H 607-.67M2 30 MICRON RP AN69 MEM?
The FDA 510(k) record lists Hospal Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL H 607-.67M2 30 MICRON RP AN69 MEM?
The FDA product code for MODEL H 607-.67M2 30 MICRON RP AN69 MEM is KDI.
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 Hospal Medical Corp. 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: KDI)
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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