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FDA 510(k)

VITAL SIGNS SALINE VASCULAR ACCESS FLUSH DEVICE

K-Number: K952645 · 1995-12-13

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

Device Summary

VITAL SIGNS SALINE 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 K952645. 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 SALINE VASCULAR ACCESS FLUSH DEVICE?

VITAL SIGNS SALINE 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 K952645.

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

VITAL SIGNS SALINE VASCULAR ACCESS FLUSH DEVICE received FDA 510(k) clearance on 1995-12-13, under 510(k) number K952645.

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

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

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Other records listing Vital Signs, Inc. as applicant

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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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