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FDA 510(k)

VISI-WIPE

K-Number: K884924 · 1989-01-31

ApplicantVisitec Co.
Decision Date1989-01-31
Product CodeHOF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISI-WIPE is the device name listed in this FDA 510(k) record. The listed applicant is Visitec Co.. It received FDA 510(k) clearance on 1989-01-31 under 510(k) number K884924. The device is classified under product code HOF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISI-WIPE?

VISI-WIPE is a medical device that received FDA 510(k) clearance on 1989-01-31. The listed applicant is Visitec Co.. The 510(k) number is K884924.

When did VISI-WIPE receive FDA 510(k) clearance?

VISI-WIPE received FDA 510(k) clearance on 1989-01-31, under 510(k) number K884924.

Who is the listed applicant for VISI-WIPE?

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 VISI-WIPE?

The FDA product code for VISI-WIPE is HOF.

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

View all 49 devices →

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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