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FDA 510(k)

DVT PREVENTION SYS. MBE 22 PRESSURE U.

K-Number: K800337 · 1980-03-25

ApplicantMed-Bio Engineering, Inc.
Decision Date1980-03-25
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DVT PREVENTION SYS. MBE 22 PRESSURE U. is the device name listed in this FDA 510(k) record. The listed applicant is Med-Bio Engineering, Inc.. It received FDA 510(k) clearance on 1980-03-25 under 510(k) number K800337. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DVT PREVENTION SYS. MBE 22 PRESSURE U.?

DVT PREVENTION SYS. MBE 22 PRESSURE U. is a medical device that received FDA 510(k) clearance on 1980-03-25. The listed applicant is Med-Bio Engineering, Inc.. The 510(k) number is K800337.

When did DVT PREVENTION SYS. MBE 22 PRESSURE U. receive FDA 510(k) clearance?

DVT PREVENTION SYS. MBE 22 PRESSURE U. received FDA 510(k) clearance on 1980-03-25, under 510(k) number K800337.

Who is the listed applicant for DVT PREVENTION SYS. MBE 22 PRESSURE U.?

The FDA 510(k) record lists Med-Bio Engineering, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DVT PREVENTION SYS. MBE 22 PRESSURE U.?

The FDA product code for DVT PREVENTION SYS. MBE 22 PRESSURE U. is JOW.

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Related Devices (Code: JOW)

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.

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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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