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FDA 510(k)

CATH CARE KIT

K-Number: K760560 · 1976-11-12

ApplicantWalpak Co.
Decision Date1976-11-12
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CATH CARE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Walpak Co.. It received FDA 510(k) clearance on 1976-11-12 under 510(k) number K760560. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATH CARE KIT?

CATH CARE KIT is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Walpak Co.. The 510(k) number is K760560.

When did CATH CARE KIT receive FDA 510(k) clearance?

CATH CARE KIT received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760560.

Who is the listed applicant for CATH CARE KIT?

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

What is the FDA product code for CATH CARE KIT?

The FDA product code for CATH CARE KIT is KGO.

Other records listing Walpak Co. as applicant

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Related Devices (Code: KGO)

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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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