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FDA 510(k)

FREQUENCY DOUBLED ND: YAG PHOTOCOAGULATOR, MODEL VITRA

K-Number: K043236 · 2005-02-07

ApplicantQuantel Medical
Decision Date2005-02-07
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FREQUENCY DOUBLED ND: YAG PHOTOCOAGULATOR, MODEL VITRA is the device name listed in this FDA 510(k) record. The listed applicant is Quantel Medical. It received FDA 510(k) clearance on 2005-02-07 under 510(k) number K043236. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREQUENCY DOUBLED ND: YAG PHOTOCOAGULATOR, MODEL VITRA?

FREQUENCY DOUBLED ND: YAG PHOTOCOAGULATOR, MODEL VITRA is a medical device that received FDA 510(k) clearance on 2005-02-07. The listed applicant is Quantel Medical. The 510(k) number is K043236.

When did FREQUENCY DOUBLED ND: YAG PHOTOCOAGULATOR, MODEL VITRA receive FDA 510(k) clearance?

FREQUENCY DOUBLED ND: YAG PHOTOCOAGULATOR, MODEL VITRA received FDA 510(k) clearance on 2005-02-07, under 510(k) number K043236.

Who is the listed applicant for FREQUENCY DOUBLED ND: YAG PHOTOCOAGULATOR, MODEL VITRA?

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

What is the FDA product code for FREQUENCY DOUBLED ND: YAG PHOTOCOAGULATOR, MODEL VITRA?

The FDA product code for FREQUENCY DOUBLED ND: YAG PHOTOCOAGULATOR, MODEL VITRA is HQF.

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Other records listing Quantel Medical 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.

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Related Devices (Code: HQF)

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.

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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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