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FDA 510(k)

PERI-PUSHER

K-Number: K953046 · 1995-09-22

ApplicantDiacor, Inc.
Decision Date1995-09-22
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PERI-PUSHER is the device name listed in this FDA 510(k) record. The listed applicant is Diacor, Inc.. It received FDA 510(k) clearance on 1995-09-22 under 510(k) number K953046. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERI-PUSHER?

PERI-PUSHER is a medical device that received FDA 510(k) clearance on 1995-09-22. The listed applicant is Diacor, Inc.. The 510(k) number is K953046.

When did PERI-PUSHER receive FDA 510(k) clearance?

PERI-PUSHER received FDA 510(k) clearance on 1995-09-22, under 510(k) number K953046.

Who is the listed applicant for PERI-PUSHER?

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

What is the FDA product code for PERI-PUSHER?

The FDA product code for PERI-PUSHER is IYE.

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Other records listing Diacor, Inc. as applicant

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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