FDA 510(k)

MOTORIZED ELECTRIC PARALLEL BARS

K-Number: K933311 · 1994-01-26

Decision Date1994-01-26

Product CodeBXB

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

MOTORIZED ELECTRIC PARALLEL BARS is the device name listed in this FDA 510(k) record. The listed applicant is Midland Mfg. Co.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K933311. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOTORIZED ELECTRIC PARALLEL BARS?

MOTORIZED ELECTRIC PARALLEL BARS is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Midland Mfg. Co.. The 510(k) number is K933311.

When did MOTORIZED ELECTRIC PARALLEL BARS receive FDA 510(k) clearance?

MOTORIZED ELECTRIC PARALLEL BARS received FDA 510(k) clearance on 1994-01-26, under 510(k) number K933311.

Who is the listed applicant for MOTORIZED ELECTRIC PARALLEL BARS?

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

What is the FDA product code for MOTORIZED ELECTRIC PARALLEL BARS?

The FDA product code for MOTORIZED ELECTRIC PARALLEL BARS is BXB.

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Other records listing Midland Mfg. Co. as applicant

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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.