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FDA 510(k)

KEITHLEY LYMPHOCYTE DEPLETION CART

K-Number: K801899 · 1980-09-26

ApplicantKeithley Development Co.
Decision Date1980-09-26
Product CodeKDK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KEITHLEY LYMPHOCYTE DEPLETION CART is the device name listed in this FDA 510(k) record. The listed applicant is Keithley Development Co.. It received FDA 510(k) clearance on 1980-09-26 under 510(k) number K801899. The device is classified under product code KDK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEITHLEY LYMPHOCYTE DEPLETION CART?

KEITHLEY LYMPHOCYTE DEPLETION CART is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is Keithley Development Co.. The 510(k) number is K801899.

When did KEITHLEY LYMPHOCYTE DEPLETION CART receive FDA 510(k) clearance?

KEITHLEY LYMPHOCYTE DEPLETION CART received FDA 510(k) clearance on 1980-09-26, under 510(k) number K801899.

Who is the listed applicant for KEITHLEY LYMPHOCYTE DEPLETION CART?

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

What is the FDA product code for KEITHLEY LYMPHOCYTE DEPLETION CART?

The FDA product code for KEITHLEY LYMPHOCYTE DEPLETION CART is KDK.

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.

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Other records listing Keithley Development 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.

K792256KEITHLEY CLAMP

Related Devices (Code: KDK)

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.

K053169RM3 RENAL PRESERVATION SYSTEMWaters Instruments, Inc.K911577HYPOTRANS MODEL 750Martin Mclane Medical

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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