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FDA 510(k)

PUSH BALL INCLINE

K-Number: K790530 · 1979-04-03

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

Device Summary

PUSH BALL INCLINE 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 K790530. The device is classified under product code ION. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PUSH BALL INCLINE?

PUSH BALL INCLINE 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 K790530.

When did PUSH BALL INCLINE receive FDA 510(k) clearance?

PUSH BALL INCLINE received FDA 510(k) clearance on 1979-04-03, under 510(k) number K790530.

Who is the listed applicant for PUSH BALL INCLINE?

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 PUSH BALL INCLINE?

The FDA product code for PUSH BALL INCLINE is ION.

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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

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Related Devices (Code: ION)

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.

K120783ABLE-XIm-Able, Ltd.K885343STANDEXAlt, Inc.K851065GRAVITY KING (DEEMED SE 87/09/18)Unique Functional ProductsK840551MOBILIZERLossing Orthopedic, Inc.K833870KNEE WALKERMaddak, Inc.K833249FITNESSFitness Equipment Co., 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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