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FDA 510(k)

ENDOGATOR ENDOSCOPY IRRIGATION PUMP, MODEL EGP-100

K-Number: K060962 · 2006-04-19

Decision Date2006-04-19
Product CodeOCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOGATOR ENDOSCOPY IRRIGATION PUMP, MODEL EGP-100 is the device name listed in this FDA 510(k) record. The listed applicant is Byrne Medical, Inc.. It received FDA 510(k) clearance on 2006-04-19 under 510(k) number K060962. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOGATOR ENDOSCOPY IRRIGATION PUMP, MODEL EGP-100?

ENDOGATOR ENDOSCOPY IRRIGATION PUMP, MODEL EGP-100 is a medical device that received FDA 510(k) clearance on 2006-04-19. The listed applicant is Byrne Medical, Inc.. The 510(k) number is K060962.

When did ENDOGATOR ENDOSCOPY IRRIGATION PUMP, MODEL EGP-100 receive FDA 510(k) clearance?

ENDOGATOR ENDOSCOPY IRRIGATION PUMP, MODEL EGP-100 received FDA 510(k) clearance on 2006-04-19, under 510(k) number K060962.

Who is the listed applicant for ENDOGATOR ENDOSCOPY IRRIGATION PUMP, MODEL EGP-100?

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

What is the FDA product code for ENDOGATOR ENDOSCOPY IRRIGATION PUMP, MODEL EGP-100?

The FDA product code for ENDOGATOR ENDOSCOPY IRRIGATION PUMP, MODEL EGP-100 is OCX.

Related Clinical Trials

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.

Other records listing Byrne Medical, 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.

View all 12 devices →

Related Devices (Code: OCX)

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.

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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