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FDA 510(k)

LAYDOWN ARM SUPPORT MECHANISM

K-Number: K885104 · 1988-12-27

Decision Date1988-12-27
Product CodeKNN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LAYDOWN ARM SUPPORT MECHANISM is the device name listed in this FDA 510(k) record. The listed applicant is Rolcontrol Products, Co., Inc.. It received FDA 510(k) clearance on 1988-12-27 under 510(k) number K885104. The device is classified under product code KNN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAYDOWN ARM SUPPORT MECHANISM?

LAYDOWN ARM SUPPORT MECHANISM is a medical device that received FDA 510(k) clearance on 1988-12-27. The listed applicant is Rolcontrol Products, Co., Inc.. The 510(k) number is K885104.

When did LAYDOWN ARM SUPPORT MECHANISM receive FDA 510(k) clearance?

LAYDOWN ARM SUPPORT MECHANISM received FDA 510(k) clearance on 1988-12-27, under 510(k) number K885104.

Who is the listed applicant for LAYDOWN ARM SUPPORT MECHANISM?

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

What is the FDA product code for LAYDOWN ARM SUPPORT MECHANISM?

The FDA product code for LAYDOWN ARM SUPPORT MECHANISM is KNN.

Related Clinical Trials

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.

Other records listing Rolcontrol Products, Co., Inc. 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: KNN)

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.

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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