Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

49-610 NIKO-NOSE FIXATION TAPE

K-Number: K902896 · 1990-10-23

Decision Date1990-10-23
Product CodeCBH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

49-610 NIKO-NOSE FIXATION TAPE is the device name listed in this FDA 510(k) record. The listed applicant is Nikomed U.S.A., Inc.. It received FDA 510(k) clearance on 1990-10-23 under 510(k) number K902896. The device is classified under product code CBH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 49-610 NIKO-NOSE FIXATION TAPE?

49-610 NIKO-NOSE FIXATION TAPE is a medical device that received FDA 510(k) clearance on 1990-10-23. The listed applicant is Nikomed U.S.A., Inc.. The 510(k) number is K902896.

When did 49-610 NIKO-NOSE FIXATION TAPE receive FDA 510(k) clearance?

49-610 NIKO-NOSE FIXATION TAPE received FDA 510(k) clearance on 1990-10-23, under 510(k) number K902896.

Who is the listed applicant for 49-610 NIKO-NOSE FIXATION TAPE?

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

What is the FDA product code for 49-610 NIKO-NOSE FIXATION TAPE?

The FDA product code for 49-610 NIKO-NOSE FIXATION TAPE is CBH.

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 Nikomed U.S.A., 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 15 devices →

Related Devices (Code: CBH)

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.

↑