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FDA 510(k)

RODENSTOCK LASER SLITLAMP

K-Number: K973220 · 1997-11-04

ApplicantG. Rodenstock Instrumente GmbH
Decision Date1997-11-04
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RODENSTOCK LASER SLITLAMP is the device name listed in this FDA 510(k) record. The listed applicant is G. Rodenstock Instrumente GmbH. It received FDA 510(k) clearance on 1997-11-04 under 510(k) number K973220. 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 RODENSTOCK LASER SLITLAMP?

RODENSTOCK LASER SLITLAMP is a medical device that received FDA 510(k) clearance on 1997-11-04. The listed applicant is G. Rodenstock Instrumente GmbH. The 510(k) number is K973220.

When did RODENSTOCK LASER SLITLAMP receive FDA 510(k) clearance?

RODENSTOCK LASER SLITLAMP received FDA 510(k) clearance on 1997-11-04, under 510(k) number K973220.

Who is the listed applicant for RODENSTOCK LASER SLITLAMP?

The FDA 510(k) record lists G. Rodenstock Instrumente GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RODENSTOCK LASER SLITLAMP?

The FDA product code for RODENSTOCK LASER SLITLAMP is HQF.

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.

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Other records listing G. Rodenstock Instrumente GmbH 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.

K871268RODENSTOCK SCANNING LASER OPHTHALMOSCOPEK864063ORION 3001, LASER PHOTOCOAGULATOR

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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