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FDA 510(k)

ARTERIAL-VENOUS COMPRESSION DRESSING

K-Number: K851489 · 1985-06-11

ApplicantMedi-Plast Intl., Inc.
Decision Date1985-06-11
Product Code
DecisionSubstantially Equivalent

Device Summary

ARTERIAL-VENOUS COMPRESSION DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Plast Intl., Inc.. It received FDA 510(k) clearance on 1985-06-11 under 510(k) number K851489. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIAL-VENOUS COMPRESSION DRESSING?

ARTERIAL-VENOUS COMPRESSION DRESSING is a medical device that received FDA 510(k) clearance on 1985-06-11. The listed applicant is Medi-Plast Intl., Inc.. The 510(k) number is K851489.

When did ARTERIAL-VENOUS COMPRESSION DRESSING receive FDA 510(k) clearance?

ARTERIAL-VENOUS COMPRESSION DRESSING received FDA 510(k) clearance on 1985-06-11, under 510(k) number K851489.

Who is the listed applicant for ARTERIAL-VENOUS COMPRESSION DRESSING?

The FDA 510(k) record lists Medi-Plast Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Medi-Plast Intl., 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.

K954284MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON)K87358810CC CONTROL SYRINGEK863402MEDI-PLAST DISPOSABLE MANIFOLDK861785FLUOROSCOPE BAND BAGK842136STERILE PAN SETK840021OPERATING ROOM TRAY SET

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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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