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FDA 510(k)

CONDUCTIVE CUSHION

K-Number: K780941 · 1978-07-27

ApplicantMarkham Service Co., Inc.
Decision Date1978-07-27
Product CodeKIC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CONDUCTIVE CUSHION is the device name listed in this FDA 510(k) record. The listed applicant is Markham Service Co., Inc.. It received FDA 510(k) clearance on 1978-07-27 under 510(k) number K780941. The device is classified under product code KIC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONDUCTIVE CUSHION?

CONDUCTIVE CUSHION is a medical device that received FDA 510(k) clearance on 1978-07-27. The listed applicant is Markham Service Co., Inc.. The 510(k) number is K780941.

When did CONDUCTIVE CUSHION receive FDA 510(k) clearance?

CONDUCTIVE CUSHION received FDA 510(k) clearance on 1978-07-27, under 510(k) number K780941.

Who is the listed applicant for CONDUCTIVE CUSHION?

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

What is the FDA product code for CONDUCTIVE CUSHION?

The FDA product code for CONDUCTIVE CUSHION is KIC.

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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Related Devices (Code: KIC)

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.

K960189GEL-T CUSHIONSpan-America Medical Systems, Inc.K953352PROTEAM CUSHIONIskra.MedK954117CUSTOMCARE SEATING SYSTEMSpan-America Medical Systems, Inc.K950085MULTICURE(R) S GEL PADMultigestion (Deutschland) GmbHK945667MICOS MICROPULSE(TM) ALTERNATING PRESSURE WHEELCHAIR CUSHIONMicos Medical SystemsK941858GEL CUSHIONHollister, Inc.

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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