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FDA 510(k)

LACIMAL INTUBATION SETS

K-Number: K831901 · 1983-07-12

ApplicantVisitec Co.
Decision Date1983-07-12
Product CodeHNL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LACIMAL INTUBATION SETS is the device name listed in this FDA 510(k) record. The listed applicant is Visitec Co.. It received FDA 510(k) clearance on 1983-07-12 under 510(k) number K831901. The device is classified under product code HNL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACIMAL INTUBATION SETS?

LACIMAL INTUBATION SETS is a medical device that received FDA 510(k) clearance on 1983-07-12. The listed applicant is Visitec Co.. The 510(k) number is K831901.

When did LACIMAL INTUBATION SETS receive FDA 510(k) clearance?

LACIMAL INTUBATION SETS received FDA 510(k) clearance on 1983-07-12, under 510(k) number K831901.

Who is the listed applicant for LACIMAL INTUBATION SETS?

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 LACIMAL INTUBATION SETS?

The FDA product code for LACIMAL INTUBATION SETS is HNL.

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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: HNL)

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.

K843491CONCEPT FIBER OPTIC CANALICULUS INTUBAConcept, Inc.K840861TSE-ANDERSON MODIFIED LACRIMAL GROOVHansen Ophthalmic Development LabK833671STERILE OIL AND GUIDEWIRECooperVision, Inc.K813187PILLING LACRIMAL INTUBATION SYSTEMNarco ScientificK812255ETHICON LACRIMAL STENTETHICON, Inc.K802845CONCEPT CANALICULUS INTUBATION SETConcept, Inc.

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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