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FDA 510(k)

SCALAMOBIL

K-Number: K920105 · 1992-08-06

ApplicantAlber Technologies, Inc.
Decision Date1992-08-06
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SCALAMOBIL is the device name listed in this FDA 510(k) record. The listed applicant is Alber Technologies, Inc.. It received FDA 510(k) clearance on 1992-08-06 under 510(k) number K920105. The device is classified under product code ING. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCALAMOBIL?

SCALAMOBIL is a medical device that received FDA 510(k) clearance on 1992-08-06. The listed applicant is Alber Technologies, Inc.. The 510(k) number is K920105.

When did SCALAMOBIL receive FDA 510(k) clearance?

SCALAMOBIL received FDA 510(k) clearance on 1992-08-06, under 510(k) number K920105.

Who is the listed applicant for SCALAMOBIL?

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

What is the FDA product code for SCALAMOBIL?

The FDA product code for SCALAMOBIL is ING.

Related Clinical Trials

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Other records listing Alber Technologies, 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.

K943789POWER WHEELCHAIR CONVERSION KIT

Related Devices (Code: ING)

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

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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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