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)

SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE

K-Number: K954438 · 1995-12-29

ApplicantRms Div.
Decision Date1995-12-29
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Rms Div.. It received FDA 510(k) clearance on 1995-12-29 under 510(k) number K954438. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE?

SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1995-12-29. The listed applicant is Rms Div.. The 510(k) number is K954438.

When did SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE receive FDA 510(k) clearance?

SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE received FDA 510(k) clearance on 1995-12-29, under 510(k) number K954438.

Who is the listed applicant for SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE?

The FDA 510(k) record lists Rms Div. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE?

The FDA product code for SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE is CCW.

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 Rms Div. 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 10 devices →

Related Devices (Code: CCW)

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.

↑