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FDA 510(k)

PERIPUMP

K-Number: K934552 · 1995-08-09

ApplicantDeschutes Medical Products, Inc.
Decision Date1995-08-09
Product CodeHIR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PERIPUMP is the device name listed in this FDA 510(k) record. The listed applicant is Deschutes Medical Products, Inc.. It received FDA 510(k) clearance on 1995-08-09 under 510(k) number K934552. The device is classified under product code HIR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIPUMP?

PERIPUMP is a medical device that received FDA 510(k) clearance on 1995-08-09. The listed applicant is Deschutes Medical Products, Inc.. The 510(k) number is K934552.

When did PERIPUMP receive FDA 510(k) clearance?

PERIPUMP received FDA 510(k) clearance on 1995-08-09, under 510(k) number K934552.

Who is the listed applicant for PERIPUMP?

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

What is the FDA product code for PERIPUMP?

The FDA product code for PERIPUMP is HIR.

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Other records listing Deschutes Medical Products, Inc. as applicant

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Related Devices (Code: HIR)

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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