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FDA 510(k)

MEDI STRUMPF

K-Number: K941926 · 1994-06-15

ApplicantMedi USA, LP
Decision Date1994-06-15
Product CodeDWL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDI STRUMPF is the device name listed in this FDA 510(k) record. The listed applicant is Medi USA, LP. It received FDA 510(k) clearance on 1994-06-15 under 510(k) number K941926. The device is classified under product code DWL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI STRUMPF?

MEDI STRUMPF is a medical device that received FDA 510(k) clearance on 1994-06-15. The listed applicant is Medi USA, LP. The 510(k) number is K941926.

When did MEDI STRUMPF receive FDA 510(k) clearance?

MEDI STRUMPF received FDA 510(k) clearance on 1994-06-15, under 510(k) number K941926.

Who is the listed applicant for MEDI STRUMPF?

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

What is the FDA product code for MEDI STRUMPF?

The FDA product code for MEDI STRUMPF is DWL.

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 Medi USA, LP 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.

Related Devices (Code: DWL)

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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