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FDA 510(k)

VYDAX 525-550 & 5100 FLUOROTELOMER

K-Number: K833357 · 1983-12-12

ApplicantETHICON, Inc.
Decision Date1983-12-12
Product CodeGDT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VYDAX 525-550 & 5100 FLUOROTELOMER is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1983-12-12 under 510(k) number K833357. The device is classified under product code GDT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VYDAX 525-550 & 5100 FLUOROTELOMER?

VYDAX 525-550 & 5100 FLUOROTELOMER is a medical device that received FDA 510(k) clearance on 1983-12-12. The listed applicant is ETHICON, Inc.. The 510(k) number is K833357.

When did VYDAX 525-550 & 5100 FLUOROTELOMER receive FDA 510(k) clearance?

VYDAX 525-550 & 5100 FLUOROTELOMER received FDA 510(k) clearance on 1983-12-12, under 510(k) number K833357.

Who is the listed applicant for VYDAX 525-550 & 5100 FLUOROTELOMER?

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

What is the FDA product code for VYDAX 525-550 & 5100 FLUOROTELOMER?

The FDA product code for VYDAX 525-550 & 5100 FLUOROTELOMER is GDT.

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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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