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FDA 510(k)

MEDITEC (RODENSTOCK) LASER PHOTOCOAGUL

K-Number: K791659 · 1979-10-11

ApplicantCoburn Optical Ind., Inc.
Decision Date1979-10-11
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MEDITEC (RODENSTOCK) LASER PHOTOCOAGUL is the device name listed in this FDA 510(k) record. The listed applicant is Coburn Optical Ind., Inc.. It received FDA 510(k) clearance on 1979-10-11 under 510(k) number K791659. 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 MEDITEC (RODENSTOCK) LASER PHOTOCOAGUL?

MEDITEC (RODENSTOCK) LASER PHOTOCOAGUL is a medical device that received FDA 510(k) clearance on 1979-10-11. The listed applicant is Coburn Optical Ind., Inc.. The 510(k) number is K791659.

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

MEDITEC (RODENSTOCK) LASER PHOTOCOAGUL received FDA 510(k) clearance on 1979-10-11, under 510(k) number K791659.

Who is the listed applicant for MEDITEC (RODENSTOCK) LASER PHOTOCOAGUL?

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

What is the FDA product code for MEDITEC (RODENSTOCK) LASER PHOTOCOAGUL?

The FDA product code for MEDITEC (RODENSTOCK) LASER PHOTOCOAGUL is HQF.

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Other records listing Coburn Optical Ind., 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.

K892347MAGNILINK SYSTEM 101K892348MAGNILINK SYSTEM 201K892350MAGNILINK SYSTEM 402/5K892349MAGNILINK SYSTEM 209K892351MAGNILINK SYSTEM 602K862188IRRIGATION & ASPIRATION/VITRECTOMY DEVICE

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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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