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FDA 510(k)

AHLBERGS KOMBI I & KOMBI II MOBILE TRANSFER CHAIRS

K-Number: K851548 · 1985-07-09

Decision Date1985-07-09
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AHLBERGS KOMBI I & KOMBI II MOBILE TRANSFER CHAIRS is the device name listed in this FDA 510(k) record. The listed applicant is Daun International, Inc.. It received FDA 510(k) clearance on 1985-07-09 under 510(k) number K851548. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AHLBERGS KOMBI I & KOMBI II MOBILE TRANSFER CHAIRS?

AHLBERGS KOMBI I & KOMBI II MOBILE TRANSFER CHAIRS is a medical device that received FDA 510(k) clearance on 1985-07-09. The listed applicant is Daun International, Inc.. The 510(k) number is K851548.

When did AHLBERGS KOMBI I & KOMBI II MOBILE TRANSFER CHAIRS receive FDA 510(k) clearance?

AHLBERGS KOMBI I & KOMBI II MOBILE TRANSFER CHAIRS received FDA 510(k) clearance on 1985-07-09, under 510(k) number K851548.

Who is the listed applicant for AHLBERGS KOMBI I & KOMBI II MOBILE TRANSFER CHAIRS?

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

What is the FDA product code for AHLBERGS KOMBI I & KOMBI II MOBILE TRANSFER CHAIRS?

The FDA product code for AHLBERGS KOMBI I & KOMBI II MOBILE TRANSFER CHAIRS is INM.

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 Daun International, 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.

View all 7 devices →

Related Devices (Code: INM)

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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