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FDA 510(k)

DRAPING MATERIAL, COLBALT 60 STERILE

K-Number: K780846 · 1978-06-19

ApplicantKimberly-Clark Corp.
Decision Date1978-06-19
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DRAPING MATERIAL, COLBALT 60 STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Kimberly-Clark Corp.. It received FDA 510(k) clearance on 1978-06-19 under 510(k) number K780846. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRAPING MATERIAL, COLBALT 60 STERILE?

DRAPING MATERIAL, COLBALT 60 STERILE is a medical device that received FDA 510(k) clearance on 1978-06-19. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K780846.

When did DRAPING MATERIAL, COLBALT 60 STERILE receive FDA 510(k) clearance?

DRAPING MATERIAL, COLBALT 60 STERILE received FDA 510(k) clearance on 1978-06-19, under 510(k) number K780846.

Who is the listed applicant for DRAPING MATERIAL, COLBALT 60 STERILE?

The FDA 510(k) record lists Kimberly-Clark Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRAPING MATERIAL, COLBALT 60 STERILE?

The FDA product code for DRAPING MATERIAL, COLBALT 60 STERILE is KKX.

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Other records listing Kimberly-Clark Corp. as applicant

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Related Devices (Code: KKX)

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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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