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FDA 510(k)

VISITEC NEDDLE TANGE (SURGERY)

K-Number: K811960 · 1981-08-07

ApplicantVisitec Co.
Decision Date1981-08-07
Product Code
DecisionSubstantially Equivalent

Device Summary

VISITEC NEDDLE TANGE (SURGERY) is the device name listed in this FDA 510(k) record. The listed applicant is Visitec Co.. It received FDA 510(k) clearance on 1981-08-07 under 510(k) number K811960. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISITEC NEDDLE TANGE (SURGERY)?

VISITEC NEDDLE TANGE (SURGERY) is a medical device that received FDA 510(k) clearance on 1981-08-07. The listed applicant is Visitec Co.. The 510(k) number is K811960.

When did VISITEC NEDDLE TANGE (SURGERY) receive FDA 510(k) clearance?

VISITEC NEDDLE TANGE (SURGERY) received FDA 510(k) clearance on 1981-08-07, under 510(k) number K811960.

Who is the listed applicant for VISITEC NEDDLE TANGE (SURGERY)?

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

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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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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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