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FDA 510(k)

ASL MODEL #102

K-Number: K914739 · 1991-12-16

ApplicantAdaptive Switch Laboratories, Inc.
Decision Date1991-12-16
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ASL MODEL #102 is the device name listed in this FDA 510(k) record. The listed applicant is Adaptive Switch Laboratories, Inc.. It received FDA 510(k) clearance on 1991-12-16 under 510(k) number K914739. 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 ASL MODEL #102?

ASL MODEL #102 is a medical device that received FDA 510(k) clearance on 1991-12-16. The listed applicant is Adaptive Switch Laboratories, Inc.. The 510(k) number is K914739.

When did ASL MODEL #102 receive FDA 510(k) clearance?

ASL MODEL #102 received FDA 510(k) clearance on 1991-12-16, under 510(k) number K914739.

Who is the listed applicant for ASL MODEL #102?

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

What is the FDA product code for ASL MODEL #102?

The FDA product code for ASL MODEL #102 is ITI.

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.

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Other records listing Adaptive Switch Laboratories, 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.

K914737ASL MODEL #104K914738ASL MODEL 101K914740ASL MODEL #103

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.

K262582Electric wheelchair (GP100)Suzhou Green Pine Medical Co., Ltd.K262054Electric WheelchairYongkang Joymax Medical Technology Co., Ltd.K260053Power Wheelchair (OS-R-M01I)Beijing OrionStar Technology Co., Ltd.K260229Electric wheelchair (HC819N, HC830N, HC831N)Yongkang Hengyi Vehicle Co., Ltd.K261354Electric wheelchair (D03)Foshan Sowell Medical Technology Co., Ltd.K261149Electric Wheelchair (DY611A-2, DY612A-1)Zhejiang Lumbre Electric Appliance Co., Ltd.

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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