FLOWTRON DVT SYSTEM AC500 PUMP, L501 GARMENT
K-Number: K881632 · 1988-09-26
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Device Summary
Frequently Asked Questions
What is the FLOWTRON DVT SYSTEM AC500 PUMP, L501 GARMENT?
FLOWTRON DVT SYSTEM AC500 PUMP, L501 GARMENT is a medical device that received FDA 510(k) clearance on 1988-09-26. The listed applicant is Huntleigh Technology, Inc.. The 510(k) number is K881632.
When did FLOWTRON DVT SYSTEM AC500 PUMP, L501 GARMENT receive FDA 510(k) clearance?
FLOWTRON DVT SYSTEM AC500 PUMP, L501 GARMENT received FDA 510(k) clearance on 1988-09-26, under 510(k) number K881632.
Who is the listed applicant for FLOWTRON DVT SYSTEM AC500 PUMP, L501 GARMENT?
The FDA 510(k) record lists Huntleigh Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLOWTRON DVT SYSTEM AC500 PUMP, L501 GARMENT?
The FDA product code for FLOWTRON DVT SYSTEM AC500 PUMP, L501 GARMENT is JOW.
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 Huntleigh Technology, 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: 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.
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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