MALLAWANY ATRAUMATIC TISSUE FORCEPS
K-Number: K922248 · 1994-02-17
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Device Summary
Frequently Asked Questions
What is the MALLAWANY ATRAUMATIC TISSUE FORCEPS?
MALLAWANY ATRAUMATIC TISSUE FORCEPS is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is Numed Technologies, Inc.. The 510(k) number is K922248.
When did MALLAWANY ATRAUMATIC TISSUE FORCEPS receive FDA 510(k) clearance?
MALLAWANY ATRAUMATIC TISSUE FORCEPS received FDA 510(k) clearance on 1994-02-17, under 510(k) number K922248.
Who is the listed applicant for MALLAWANY ATRAUMATIC TISSUE FORCEPS?
The FDA 510(k) record lists Numed Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MALLAWANY ATRAUMATIC TISSUE FORCEPS?
The FDA product code for MALLAWANY ATRAUMATIC TISSUE FORCEPS is HET.
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 Numed Technologies, 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.
Related Devices (Code: HET)
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
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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