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FDA 510(k)

PORTABLE STANDARD

K-Number: K934263 · 1993-11-01

ApplicantCloverleaf Cycle Co.
Decision Date1993-11-01
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PORTABLE STANDARD is the device name listed in this FDA 510(k) record. The listed applicant is Cloverleaf Cycle Co.. It received FDA 510(k) clearance on 1993-11-01 under 510(k) number K934263. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTABLE STANDARD?

PORTABLE STANDARD is a medical device that received FDA 510(k) clearance on 1993-11-01. The listed applicant is Cloverleaf Cycle Co.. The 510(k) number is K934263.

When did PORTABLE STANDARD receive FDA 510(k) clearance?

PORTABLE STANDARD received FDA 510(k) clearance on 1993-11-01, under 510(k) number K934263.

Who is the listed applicant for PORTABLE STANDARD?

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

What is the FDA product code for PORTABLE STANDARD?

The FDA product code for PORTABLE STANDARD is IOR.

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Related Devices (Code: IOR)

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

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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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