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FDA 510(k)

REF. 4102CV INTERMEDIARY TUBING, REF. 4509CV STERILE ZONE KIT

K-Number: K951843 · 1995-07-14

Decision Date1995-07-14
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

REF. 4102CV INTERMEDIARY TUBING, REF. 4509CV STERILE ZONE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Future Medical Systems, Inc.. It received FDA 510(k) clearance on 1995-07-14 under 510(k) number K951843. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REF. 4102CV INTERMEDIARY TUBING, REF. 4509CV STERILE ZONE KIT?

REF. 4102CV INTERMEDIARY TUBING, REF. 4509CV STERILE ZONE KIT is a medical device that received FDA 510(k) clearance on 1995-07-14. The listed applicant is Future Medical Systems, Inc.. The 510(k) number is K951843.

When did REF. 4102CV INTERMEDIARY TUBING, REF. 4509CV STERILE ZONE KIT receive FDA 510(k) clearance?

REF. 4102CV INTERMEDIARY TUBING, REF. 4509CV STERILE ZONE KIT received FDA 510(k) clearance on 1995-07-14, under 510(k) number K951843.

Who is the listed applicant for REF. 4102CV INTERMEDIARY TUBING, REF. 4509CV STERILE ZONE KIT?

The FDA 510(k) record lists Future Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REF. 4102CV INTERMEDIARY TUBING, REF. 4509CV STERILE ZONE KIT?

The FDA product code for REF. 4102CV INTERMEDIARY TUBING, REF. 4509CV STERILE ZONE KIT is HRX.

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 Future Medical Systems, 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.

View all 12 devices →

Related Devices (Code: HRX)

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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