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FDA 510(k)

PERIPHERAL VASCULAR LABORATORY ASSISTANT MODEL 101

K-Number: K875118 · 1988-05-16

ApplicantBloodflow Laboratory, Inc.
Decision Date1988-05-16
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERIPHERAL VASCULAR LABORATORY ASSISTANT MODEL 101 is the device name listed in this FDA 510(k) record. The listed applicant is Bloodflow Laboratory, Inc.. It received FDA 510(k) clearance on 1988-05-16 under 510(k) number K875118. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIPHERAL VASCULAR LABORATORY ASSISTANT MODEL 101?

PERIPHERAL VASCULAR LABORATORY ASSISTANT MODEL 101 is a medical device that received FDA 510(k) clearance on 1988-05-16. The listed applicant is Bloodflow Laboratory, Inc.. The 510(k) number is K875118.

When did PERIPHERAL VASCULAR LABORATORY ASSISTANT MODEL 101 receive FDA 510(k) clearance?

PERIPHERAL VASCULAR LABORATORY ASSISTANT MODEL 101 received FDA 510(k) clearance on 1988-05-16, under 510(k) number K875118.

Who is the listed applicant for PERIPHERAL VASCULAR LABORATORY ASSISTANT MODEL 101?

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

What is the FDA product code for PERIPHERAL VASCULAR LABORATORY ASSISTANT MODEL 101?

The FDA product code for PERIPHERAL VASCULAR LABORATORY ASSISTANT MODEL 101 is JOM.

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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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