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FDA 510(k)

UNISTEP CAPILLARY BLOOD COLLECTION SYSTEM

K-Number: K875354 · 1988-02-17

ApplicantUlster Scientific, Inc.
Decision Date1988-02-17
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

UNISTEP CAPILLARY BLOOD COLLECTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ulster Scientific, Inc.. It received FDA 510(k) clearance on 1988-02-17 under 510(k) number K875354. The device is classified under product code LCP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNISTEP CAPILLARY BLOOD COLLECTION SYSTEM?

UNISTEP CAPILLARY BLOOD COLLECTION SYSTEM is a medical device that received FDA 510(k) clearance on 1988-02-17. The listed applicant is Ulster Scientific, Inc.. The 510(k) number is K875354.

When did UNISTEP CAPILLARY BLOOD COLLECTION SYSTEM receive FDA 510(k) clearance?

UNISTEP CAPILLARY BLOOD COLLECTION SYSTEM received FDA 510(k) clearance on 1988-02-17, under 510(k) number K875354.

Who is the listed applicant for UNISTEP CAPILLARY BLOOD COLLECTION SYSTEM?

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

What is the FDA product code for UNISTEP CAPILLARY BLOOD COLLECTION SYSTEM?

The FDA product code for UNISTEP CAPILLARY BLOOD COLLECTION SYSTEM is LCP.

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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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