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FDA 510(k)

CARROLL HEALTHCARE DLX 2300-111 ELECTRIC BED

K-Number: K962250 · 1996-10-21

ApplicantCarroll Healthcare, Inc.
Decision Date1996-10-21
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CARROLL HEALTHCARE DLX 2300-111 ELECTRIC BED is the device name listed in this FDA 510(k) record. The listed applicant is Carroll Healthcare, Inc.. It received FDA 510(k) clearance on 1996-10-21 under 510(k) number K962250. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARROLL HEALTHCARE DLX 2300-111 ELECTRIC BED?

CARROLL HEALTHCARE DLX 2300-111 ELECTRIC BED is a medical device that received FDA 510(k) clearance on 1996-10-21. The listed applicant is Carroll Healthcare, Inc.. The 510(k) number is K962250.

When did CARROLL HEALTHCARE DLX 2300-111 ELECTRIC BED receive FDA 510(k) clearance?

CARROLL HEALTHCARE DLX 2300-111 ELECTRIC BED received FDA 510(k) clearance on 1996-10-21, under 510(k) number K962250.

Who is the listed applicant for CARROLL HEALTHCARE DLX 2300-111 ELECTRIC BED?

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

What is the FDA product code for CARROLL HEALTHCARE DLX 2300-111 ELECTRIC BED?

The FDA product code for CARROLL HEALTHCARE DLX 2300-111 ELECTRIC BED is FNL.

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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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