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FDA 510(k)

PPCID- PNEUMATIC PERIPHERAL CIRCULATION IMPROVEMENT (FOOTREST) DEVICE

K-Number: K000655 · 2001-03-26

ApplicantAhava Stein
Decision Date2001-03-26
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PPCID- PNEUMATIC PERIPHERAL CIRCULATION IMPROVEMENT (FOOTREST) DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Ahava Stein. It received FDA 510(k) clearance on 2001-03-26 under 510(k) number K000655. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PPCID- PNEUMATIC PERIPHERAL CIRCULATION IMPROVEMENT (FOOTREST) DEVICE?

PPCID- PNEUMATIC PERIPHERAL CIRCULATION IMPROVEMENT (FOOTREST) DEVICE is a medical device that received FDA 510(k) clearance on 2001-03-26. The listed applicant is Ahava Stein. The 510(k) number is K000655.

When did PPCID- PNEUMATIC PERIPHERAL CIRCULATION IMPROVEMENT (FOOTREST) DEVICE receive FDA 510(k) clearance?

PPCID- PNEUMATIC PERIPHERAL CIRCULATION IMPROVEMENT (FOOTREST) DEVICE received FDA 510(k) clearance on 2001-03-26, under 510(k) number K000655.

Who is the listed applicant for PPCID- PNEUMATIC PERIPHERAL CIRCULATION IMPROVEMENT (FOOTREST) DEVICE?

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

What is the FDA product code for PPCID- PNEUMATIC PERIPHERAL CIRCULATION IMPROVEMENT (FOOTREST) DEVICE?

The FDA product code for PPCID- PNEUMATIC PERIPHERAL CIRCULATION IMPROVEMENT (FOOTREST) DEVICE is IRP.

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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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