FDA 510(k)

CUTANEOUS PRESSURE PLETHYSMOGRAPH

K-Number: K822522 · 1982-09-28

ApplicantLife Sciences Manufacturing, Inc.

Decision Date1982-09-28

Product CodeDSB

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CUTANEOUS PRESSURE PLETHYSMOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Life Sciences Manufacturing, Inc.. It received FDA 510(k) clearance on 1982-09-28 under 510(k) number K822522. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUTANEOUS PRESSURE PLETHYSMOGRAPH?

CUTANEOUS PRESSURE PLETHYSMOGRAPH is a medical device that received FDA 510(k) clearance on 1982-09-28. The listed applicant is Life Sciences Manufacturing, Inc.. The 510(k) number is K822522.

When did CUTANEOUS PRESSURE PLETHYSMOGRAPH receive FDA 510(k) clearance?

CUTANEOUS PRESSURE PLETHYSMOGRAPH received FDA 510(k) clearance on 1982-09-28, under 510(k) number K822522.

Who is the listed applicant for CUTANEOUS PRESSURE PLETHYSMOGRAPH?

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

What is the FDA product code for CUTANEOUS PRESSURE PLETHYSMOGRAPH?

The FDA product code for CUTANEOUS PRESSURE PLETHYSMOGRAPH is DSB.

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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.