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FDA 510(k)

REMOVABLE BATTERY POWER SYSTEM

K-Number: K885106 · 1988-12-27

ApplicantRolcontrol Products, Co., Inc.
Decision Date1988-12-27
Product CodeKNN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

REMOVABLE BATTERY POWER SYSTEM 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 K885106. 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 REMOVABLE BATTERY POWER SYSTEM?

REMOVABLE BATTERY POWER SYSTEM 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 K885106.

When did REMOVABLE BATTERY POWER SYSTEM receive FDA 510(k) clearance?

REMOVABLE BATTERY POWER SYSTEM received FDA 510(k) clearance on 1988-12-27, under 510(k) number K885106.

Who is the listed applicant for REMOVABLE BATTERY POWER SYSTEM?

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 REMOVABLE BATTERY POWER SYSTEM?

The FDA product code for REMOVABLE BATTERY POWER SYSTEM is KNN.

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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.

K885104LAYDOWN ARM SUPPORT MECHANISMK8851031600 LIGHT TOUCH CONTROLK885105SLIDING ARM SUPPORTK883673POWER MECHANICAL RECLINERK883679WHEELS-OFF QUICK RELEASE AXLE SYSTEMK883672PARALYZED VETERANS OF AMERICA POWER RECLINER

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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.

K211919KISS Dynamic Back Support, KISS Dynamic Solid Drop SeatKinetic Innovative Seating System, LLCK942309DYNASTY U1-31 (GELL/CELL)Foley & LardnerK942311DYNASTY U1-33 AGMFoley & LardnerK942308DYNASTY GC 12400 (GELL/CELL)Foley & LardnerK942310DYNASTY GC 12550 (GELL/CELL)Foley & LardnerK942312ALDEN LINEAGE WHEELCHAIR CUSHIONLewis W. Ward

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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