FDA 510(k)

ANSPACH ANGLED MICRONOSE ATTACHMENT

K-Number: K002903 · 2000-10-24

Decision Date2000-10-24

Product CodeHBE

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

ANSPACH ANGLED MICRONOSE ATTACHMENT is the device name listed in this FDA 510(k) record. The listed applicant is The Anspach Effort, Inc.. It received FDA 510(k) clearance on 2000-10-24 under 510(k) number K002903. The device is classified under product code HBE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANSPACH ANGLED MICRONOSE ATTACHMENT?

ANSPACH ANGLED MICRONOSE ATTACHMENT is a medical device that received FDA 510(k) clearance on 2000-10-24. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K002903.

When did ANSPACH ANGLED MICRONOSE ATTACHMENT receive FDA 510(k) clearance?

ANSPACH ANGLED MICRONOSE ATTACHMENT received FDA 510(k) clearance on 2000-10-24, under 510(k) number K002903.

Who is the listed applicant for ANSPACH ANGLED MICRONOSE ATTACHMENT?

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

What is the FDA product code for ANSPACH ANGLED MICRONOSE ATTACHMENT?

The FDA product code for ANSPACH ANGLED MICRONOSE ATTACHMENT is HBE.

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Other records listing The Anspach Effort, Inc. 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.