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FDA 510(k)

RABBIT MOBILE STANDING FRAME

K-Number: K030882 · 2003-04-04

ApplicantR82 A/S
Decision Date2003-04-04
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RABBIT MOBILE STANDING FRAME is the device name listed in this FDA 510(k) record. The listed applicant is R82 A/S. It received FDA 510(k) clearance on 2003-04-04 under 510(k) number K030882. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RABBIT MOBILE STANDING FRAME?

RABBIT MOBILE STANDING FRAME is a medical device that received FDA 510(k) clearance on 2003-04-04. The listed applicant is R82 A/S. The 510(k) number is K030882.

When did RABBIT MOBILE STANDING FRAME receive FDA 510(k) clearance?

RABBIT MOBILE STANDING FRAME received FDA 510(k) clearance on 2003-04-04, under 510(k) number K030882.

Who is the listed applicant for RABBIT MOBILE STANDING FRAME?

The FDA 510(k) record lists R82 A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RABBIT MOBILE STANDING FRAME?

The FDA product code for RABBIT MOBILE STANDING FRAME is IPL.

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Other records listing R82 A/S 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.

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Related Devices (Code: IPL)

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

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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