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FDA 510(k)

PERIPHERAL PULSE FUNCTION BLOCKS

K-Number: K810171 · 1981-02-25

ApplicantHoneywell, Inc.
Decision Date1981-02-25
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERIPHERAL PULSE FUNCTION BLOCKS is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1981-02-25 under 510(k) number K810171. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIPHERAL PULSE FUNCTION BLOCKS?

PERIPHERAL PULSE FUNCTION BLOCKS is a medical device that received FDA 510(k) clearance on 1981-02-25. The listed applicant is Honeywell, Inc.. The 510(k) number is K810171.

When did PERIPHERAL PULSE FUNCTION BLOCKS receive FDA 510(k) clearance?

PERIPHERAL PULSE FUNCTION BLOCKS received FDA 510(k) clearance on 1981-02-25, under 510(k) number K810171.

Who is the listed applicant for PERIPHERAL PULSE FUNCTION BLOCKS?

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

What is the FDA product code for PERIPHERAL PULSE FUNCTION BLOCKS?

The FDA product code for PERIPHERAL PULSE FUNCTION BLOCKS is DSK.

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Related Devices (Code: DSK)

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.

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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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