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FDA 510(k)

SPIROBAC ADAPTERS

K-Number: K944124 · 1994-09-08

ApplicantMallinckrodt Medical
Decision Date1994-09-08
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SPIROBAC ADAPTERS is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Medical. It received FDA 510(k) clearance on 1994-09-08 under 510(k) number K944124. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPIROBAC ADAPTERS?

SPIROBAC ADAPTERS is a medical device that received FDA 510(k) clearance on 1994-09-08. The listed applicant is Mallinckrodt Medical. The 510(k) number is K944124.

When did SPIROBAC ADAPTERS receive FDA 510(k) clearance?

SPIROBAC ADAPTERS received FDA 510(k) clearance on 1994-09-08, under 510(k) number K944124.

Who is the listed applicant for SPIROBAC ADAPTERS?

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

What is the FDA product code for SPIROBAC ADAPTERS?

The FDA product code for SPIROBAC ADAPTERS is CAH.

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Other records listing Mallinckrodt Medical as applicant

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Related Devices (Code: CAH)

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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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