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FDA 510(k)

CERSA-CANE

K-Number: K790558 · 1979-04-03

ApplicantMaddak, Inc.
Decision Date1979-04-03
Product CodeIPS
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CERSA-CANE is the device name listed in this FDA 510(k) record. The listed applicant is Maddak, Inc.. It received FDA 510(k) clearance on 1979-04-03 under 510(k) number K790558. The device is classified under product code IPS. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERSA-CANE?

CERSA-CANE is a medical device that received FDA 510(k) clearance on 1979-04-03. The listed applicant is Maddak, Inc.. The 510(k) number is K790558.

When did CERSA-CANE receive FDA 510(k) clearance?

CERSA-CANE received FDA 510(k) clearance on 1979-04-03, under 510(k) number K790558.

Who is the listed applicant for CERSA-CANE?

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

What is the FDA product code for CERSA-CANE?

The FDA product code for CERSA-CANE is IPS.

Related Clinical Trials

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Other records listing Maddak, 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.

K841700WALK & ROLLK841698HEAT PACKK841695CRAWLERK841693STANDING FRAMEK841697HYDRO-THERO PADK841692PRONE STANDER

View all 51 devices →

Related Devices (Code: IPS)

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.

K832969WALKING CANEMaddak, Inc.K832970CANE REACHERMaddak, Inc.K821402LIGHT WEIGHT ALUMINUM CANESManuco Manufacturing Co., Inc.K790561OFFSET ALUMINUM CANEMaddak, Inc.K790299FOREARM-CANEGuardian Products Co., Inc.K780085CANE/REACHERFred Sammons, Inc.

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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