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FDA 510(k)

LASER AND EMPHASIS SCLEROSTOMY TIP

K-Number: K926470 · 1993-07-22

ApplicantSummit Technology, Inc.
Decision Date1993-07-22
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LASER AND EMPHASIS SCLEROSTOMY TIP is the device name listed in this FDA 510(k) record. The listed applicant is Summit Technology, Inc.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K926470. 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 LASER AND EMPHASIS SCLEROSTOMY TIP?

LASER AND EMPHASIS SCLEROSTOMY TIP is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Summit Technology, Inc.. The 510(k) number is K926470.

When did LASER AND EMPHASIS SCLEROSTOMY TIP receive FDA 510(k) clearance?

LASER AND EMPHASIS SCLEROSTOMY TIP received FDA 510(k) clearance on 1993-07-22, under 510(k) number K926470.

Who is the listed applicant for LASER AND EMPHASIS SCLEROSTOMY TIP?

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

What is the FDA product code for LASER AND EMPHASIS SCLEROSTOMY TIP?

The FDA product code for LASER AND EMPHASIS SCLEROSTOMY TIP is HQF.

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Other records listing Summit Technology, 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.

K980675SUMMIT KRUMEICH-BARRAQUER MICROKERATOMEK915651OMNIMED HOLMIUM LASER AND DELIVERY SYSTEMK912522OMNIVIEW(TM) OPHTHALMIC FIBERENDO W/NEEDLEHOLDERK904470SUMMIT TECH 19/20 GAUGE OPHTHALMIC FIBERENDOSCOPE

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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