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FDA 510(k)

VICO MICRO SURGICAL INSTRUMENTS

K-Number: K843592 · 1984-10-05

ApplicantVisitec Co.
Decision Date1984-10-05
Product CodeHWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VICO MICRO SURGICAL INSTRUMENTS 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 K843592. The device is classified under product code HWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VICO MICRO SURGICAL INSTRUMENTS?

VICO MICRO SURGICAL INSTRUMENTS 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 K843592.

When did VICO MICRO SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

VICO MICRO SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1984-10-05, under 510(k) number K843592.

Who is the listed applicant for VICO MICRO SURGICAL INSTRUMENTS?

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 VICO MICRO SURGICAL INSTRUMENTS?

The FDA product code for VICO MICRO SURGICAL INSTRUMENTS is HWQ.

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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: HWQ)

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.

K970360MITEK SUTURE RETROGRADERMitek ProductsK920621ACUFEX PASSING PINS AND SURGICAL WIREAcufex Microsurgical, Inc.K923381SOFT TISSUE EXPANDERAcufex Microsurgical, Inc.K885311MENISCUS MENDER II LOOPInstrument Makar, Inc.K841622SOFT-TISSUE INSTRUMENTPlastafil, Inc.K841623SLOTTED SOFT-TISSUE INSTRUMENTPlastafil, 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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