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FDA 510(k)

KEITHLEY CLAMP

K-Number: K792256 · 1979-12-06

ApplicantKeithley Development Co.
Decision Date1979-12-06
Product CodeEYR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KEITHLEY CLAMP 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 1979-12-06 under 510(k) number K792256. The device is classified under product code EYR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEITHLEY CLAMP?

KEITHLEY CLAMP is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is Keithley Development Co.. The 510(k) number is K792256.

When did KEITHLEY CLAMP receive FDA 510(k) clearance?

KEITHLEY CLAMP received FDA 510(k) clearance on 1979-12-06, under 510(k) number K792256.

Who is the listed applicant for KEITHLEY CLAMP?

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 CLAMP?

The FDA product code for KEITHLEY CLAMP is EYR.

Related Clinical Trials

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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.

K801899KEITHLEY LYMPHOCYTE DEPLETION CART

Related Devices (Code: EYR)

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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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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