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FDA 510(k)

BUSSE HOSPITAL DISPOSABLES SPINAL MANOMETER

K-Number: K032432 · 2003-08-28

ApplicantBusse Hospital Disposables, Inc.
Decision Date2003-08-28
Product CodeFMJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BUSSE HOSPITAL DISPOSABLES SPINAL MANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Busse Hospital Disposables, Inc.. It received FDA 510(k) clearance on 2003-08-28 under 510(k) number K032432. The device is classified under product code FMJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUSSE HOSPITAL DISPOSABLES SPINAL MANOMETER?

BUSSE HOSPITAL DISPOSABLES SPINAL MANOMETER is a medical device that received FDA 510(k) clearance on 2003-08-28. The listed applicant is Busse Hospital Disposables, Inc.. The 510(k) number is K032432.

When did BUSSE HOSPITAL DISPOSABLES SPINAL MANOMETER receive FDA 510(k) clearance?

BUSSE HOSPITAL DISPOSABLES SPINAL MANOMETER received FDA 510(k) clearance on 2003-08-28, under 510(k) number K032432.

Who is the listed applicant for BUSSE HOSPITAL DISPOSABLES SPINAL MANOMETER?

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

What is the FDA product code for BUSSE HOSPITAL DISPOSABLES SPINAL MANOMETER?

The FDA product code for BUSSE HOSPITAL DISPOSABLES SPINAL MANOMETER is FMJ.

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Other records listing Busse Hospital Disposables, Inc. as applicant

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Related Devices (Code: FMJ)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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