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FDA 510(k)

ELLMAN VAPOR-VAC II

K-Number: K944558 · 1995-04-28

ApplicantNorth American Technical Services Corp.
Decision Date1995-04-28
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELLMAN VAPOR-VAC II is the device name listed in this FDA 510(k) record. The listed applicant is North American Technical Services Corp.. It received FDA 510(k) clearance on 1995-04-28 under 510(k) number K944558. 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 ELLMAN VAPOR-VAC II?

ELLMAN VAPOR-VAC II is a medical device that received FDA 510(k) clearance on 1995-04-28. The listed applicant is North American Technical Services Corp.. The 510(k) number is K944558.

When did ELLMAN VAPOR-VAC II receive FDA 510(k) clearance?

ELLMAN VAPOR-VAC II received FDA 510(k) clearance on 1995-04-28, under 510(k) number K944558.

Who is the listed applicant for ELLMAN VAPOR-VAC II?

The FDA 510(k) record lists North American Technical Services Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELLMAN VAPOR-VAC II?

The FDA product code for ELLMAN VAPOR-VAC II is GEX. This falls under the Gastroenterology category.

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Other records listing North American Technical Services Corp. as applicant

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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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