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FDA 510(k)

MEGABEAM ASPIRATING ENDOCULAR PROBE

K-Number: K952340 · 1995-06-12

ApplicantCeram Optec, Inc.
Decision Date1995-06-12
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEGABEAM ASPIRATING ENDOCULAR PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Ceram Optec, Inc.. It received FDA 510(k) clearance on 1995-06-12 under 510(k) number K952340. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEGABEAM ASPIRATING ENDOCULAR PROBE?

MEGABEAM ASPIRATING ENDOCULAR PROBE is a medical device that received FDA 510(k) clearance on 1995-06-12. The listed applicant is Ceram Optec, Inc.. The 510(k) number is K952340.

When did MEGABEAM ASPIRATING ENDOCULAR PROBE receive FDA 510(k) clearance?

MEGABEAM ASPIRATING ENDOCULAR PROBE received FDA 510(k) clearance on 1995-06-12, under 510(k) number K952340.

Who is the listed applicant for MEGABEAM ASPIRATING ENDOCULAR PROBE?

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

What is the FDA product code for MEGABEAM ASPIRATING ENDOCULAR PROBE?

The FDA product code for MEGABEAM ASPIRATING ENDOCULAR PROBE is GEX. This falls under the Gastroenterology category.

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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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