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FDA 510(k)

MODEL H 607-.67M2 30 MICRON RP AN69 MEM

K-Number: K800536 · 1980-08-07

Decision Date1980-08-07
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODEL H 607-.67M2 30 MICRON RP AN69 MEM is the device name listed in this FDA 510(k) record. The listed applicant is Hospal Medical Corp.. It received FDA 510(k) clearance on 1980-08-07 under 510(k) number K800536. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 55 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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