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FDA 510(k)

SAFETY PLUS MODEL 501

K-Number: K881051 · 1988-03-21

ApplicantSafety Rehab Systems, Inc.
Decision Date1988-03-21
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SAFETY PLUS MODEL 501 is the device name listed in this FDA 510(k) record. The listed applicant is Safety Rehab Systems, Inc.. It received FDA 510(k) clearance on 1988-03-21 under 510(k) number K881051. 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 SAFETY PLUS MODEL 501?

SAFETY PLUS MODEL 501 is a medical device that received FDA 510(k) clearance on 1988-03-21. The listed applicant is Safety Rehab Systems, Inc.. The 510(k) number is K881051.

When did SAFETY PLUS MODEL 501 receive FDA 510(k) clearance?

SAFETY PLUS MODEL 501 received FDA 510(k) clearance on 1988-03-21, under 510(k) number K881051.

Who is the listed applicant for SAFETY PLUS MODEL 501?

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

What is the FDA product code for SAFETY PLUS MODEL 501?

The FDA product code for SAFETY PLUS MODEL 501 is IOR.

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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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