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FDA 510(k)

VISITEC FLIERINGA-LEGRAND FIXATION RING

K-Number: K843195 · 1984-10-05

ApplicantVisitec Co.
Decision Date1984-10-05
Product CodeHMH
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISITEC FLIERINGA-LEGRAND FIXATION RING is the device name listed in this FDA 510(k) record. The listed applicant is Visitec Co.. It received FDA 510(k) clearance on 1984-10-05 under 510(k) number K843195. The device is classified under product code HMH. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISITEC FLIERINGA-LEGRAND FIXATION RING?

VISITEC FLIERINGA-LEGRAND FIXATION RING is a medical device that received FDA 510(k) clearance on 1984-10-05. The listed applicant is Visitec Co.. The 510(k) number is K843195.

When did VISITEC FLIERINGA-LEGRAND FIXATION RING receive FDA 510(k) clearance?

VISITEC FLIERINGA-LEGRAND FIXATION RING received FDA 510(k) clearance on 1984-10-05, under 510(k) number K843195.

Who is the listed applicant for VISITEC FLIERINGA-LEGRAND FIXATION RING?

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

What is the FDA product code for VISITEC FLIERINGA-LEGRAND FIXATION RING?

The FDA product code for VISITEC FLIERINGA-LEGRAND FIXATION RING is HMH.

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Other records listing Visitec Co. 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.

K953394VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}K945114VISITEC SCLERAL PLUGK945738VISIFLEX OPHTHALMIC SURGICAL INCISE DRAPEK945172VISITEC SILICONE RETINAL IMPLANTS/EXPLANTSK942234VISITEC PRECISE-POINTK934269FIBEROPTIC ILLUMINATED INSTRUMENTS

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Related Devices (Code: HMH)

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.

K844364SKIASCOPIC RACKSLuneau Laboratories

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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