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FDA 510(k)

SUPER-SPIKE TRANSFER SET

K-Number: K802940 · 1981-01-15

Decision Date1981-01-15
Product CodeKSB
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SUPER-SPIKE TRANSFER SET is the device name listed in this FDA 510(k) record. The listed applicant is Geneva Laboratories, Inc.. It received FDA 510(k) clearance on 1981-01-15 under 510(k) number K802940. The device is classified under product code KSB. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPER-SPIKE TRANSFER SET?

SUPER-SPIKE TRANSFER SET is a medical device that received FDA 510(k) clearance on 1981-01-15. The listed applicant is Geneva Laboratories, Inc.. The 510(k) number is K802940.

When did SUPER-SPIKE TRANSFER SET receive FDA 510(k) clearance?

SUPER-SPIKE TRANSFER SET received FDA 510(k) clearance on 1981-01-15, under 510(k) number K802940.

Who is the listed applicant for SUPER-SPIKE TRANSFER SET?

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

What is the FDA product code for SUPER-SPIKE TRANSFER SET?

The FDA product code for SUPER-SPIKE TRANSFER SET is KSB.

Related Clinical Trials

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.

Other records listing Geneva Laboratories, Inc. 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.

View all 13 devices →

Related Devices (Code: KSB)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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