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FDA 510(k)

BIO CLINIC UNDER PATIENT SCALE

K-Number: K925112 · 1993-06-18

ApplicantSunrise Medical, Inc.
Decision Date1993-06-18
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BIO CLINIC UNDER PATIENT SCALE is the device name listed in this FDA 510(k) record. The listed applicant is Sunrise Medical, Inc.. It received FDA 510(k) clearance on 1993-06-18 under 510(k) number K925112. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIO CLINIC UNDER PATIENT SCALE?

BIO CLINIC UNDER PATIENT SCALE is a medical device that received FDA 510(k) clearance on 1993-06-18. The listed applicant is Sunrise Medical, Inc.. The 510(k) number is K925112.

When did BIO CLINIC UNDER PATIENT SCALE receive FDA 510(k) clearance?

BIO CLINIC UNDER PATIENT SCALE received FDA 510(k) clearance on 1993-06-18, under 510(k) number K925112.

Who is the listed applicant for BIO CLINIC UNDER PATIENT SCALE?

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

What is the FDA product code for BIO CLINIC UNDER PATIENT SCALE?

The FDA product code for BIO CLINIC UNDER PATIENT SCALE is FRN.

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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.

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