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FDA 510(k)

1600 LIGHT TOUCH CONTROL

K-Number: K885103 · 1988-12-27

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

Device Summary

1600 LIGHT TOUCH CONTROL 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 K885103. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1600 LIGHT TOUCH CONTROL?

1600 LIGHT TOUCH CONTROL 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 K885103.

When did 1600 LIGHT TOUCH CONTROL receive FDA 510(k) clearance?

1600 LIGHT TOUCH CONTROL received FDA 510(k) clearance on 1988-12-27, under 510(k) number K885103.

Who is the listed applicant for 1600 LIGHT TOUCH CONTROL?

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 1600 LIGHT TOUCH CONTROL?

The FDA product code for 1600 LIGHT TOUCH CONTROL is ITI.

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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.

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Related Devices (Code: ITI)

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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