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FDA 510(k)

VITAL SIGNS HEPARIN VASCULAR ACCESS FLUSH DEVICE

K-Number: K953120 · 1995-12-13

ApplicantVital Signs, Inc.
Decision Date1995-12-13
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITAL SIGNS HEPARIN VASCULAR ACCESS FLUSH DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Vital Signs, Inc.. It received FDA 510(k) clearance on 1995-12-13 under 510(k) number K953120. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITAL SIGNS HEPARIN VASCULAR ACCESS FLUSH DEVICE?

VITAL SIGNS HEPARIN VASCULAR ACCESS FLUSH DEVICE is a medical device that received FDA 510(k) clearance on 1995-12-13. The listed applicant is Vital Signs, Inc.. The 510(k) number is K953120.

When did VITAL SIGNS HEPARIN VASCULAR ACCESS FLUSH DEVICE receive FDA 510(k) clearance?

VITAL SIGNS HEPARIN VASCULAR ACCESS FLUSH DEVICE received FDA 510(k) clearance on 1995-12-13, under 510(k) number K953120.

Who is the listed applicant for VITAL SIGNS HEPARIN VASCULAR ACCESS FLUSH DEVICE?

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

What is the FDA product code for VITAL SIGNS HEPARIN VASCULAR ACCESS FLUSH DEVICE?

The FDA product code for VITAL SIGNS HEPARIN VASCULAR ACCESS FLUSH DEVICE is FOZ.

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Other records listing Vital Signs, Inc. as applicant

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Related Devices (Code: FOZ)

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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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