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FDA 510(k)

B.A.C. 1000 MOBILE STANDING DEVICE

K-Number: K884840 · 1989-03-15

ApplicantLuconex, Inc.
Decision Date1989-03-15
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

B.A.C. 1000 MOBILE STANDING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Luconex, Inc.. It received FDA 510(k) clearance on 1989-03-15 under 510(k) number K884840. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the B.A.C. 1000 MOBILE STANDING DEVICE?

B.A.C. 1000 MOBILE STANDING DEVICE is a medical device that received FDA 510(k) clearance on 1989-03-15. The listed applicant is Luconex, Inc.. The 510(k) number is K884840.

When did B.A.C. 1000 MOBILE STANDING DEVICE receive FDA 510(k) clearance?

B.A.C. 1000 MOBILE STANDING DEVICE received FDA 510(k) clearance on 1989-03-15, under 510(k) number K884840.

Who is the listed applicant for B.A.C. 1000 MOBILE STANDING DEVICE?

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

What is the FDA product code for B.A.C. 1000 MOBILE STANDING DEVICE?

The FDA product code for B.A.C. 1000 MOBILE STANDING DEVICE is IPL.

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 Luconex, 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.

K896904B.A.C. 3000 CHAIR/STANDER

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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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