BLOM-SINGER VOICE PROSTHESIS FLUSHING PIPET
K-Number: K932163 · 1993-12-15
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Device Summary
Frequently Asked Questions
What is the BLOM-SINGER VOICE PROSTHESIS FLUSHING PIPET?
BLOM-SINGER VOICE PROSTHESIS FLUSHING PIPET is a medical device that received FDA 510(k) clearance on 1993-12-15. The listed applicant is Helix Medical, Inc.. The 510(k) number is K932163.
When did BLOM-SINGER VOICE PROSTHESIS FLUSHING PIPET receive FDA 510(k) clearance?
BLOM-SINGER VOICE PROSTHESIS FLUSHING PIPET received FDA 510(k) clearance on 1993-12-15, under 510(k) number K932163.
Who is the listed applicant for BLOM-SINGER VOICE PROSTHESIS FLUSHING PIPET?
The FDA 510(k) record lists Helix Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOM-SINGER VOICE PROSTHESIS FLUSHING PIPET?
The FDA product code for BLOM-SINGER VOICE PROSTHESIS FLUSHING PIPET is EWL.
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 Helix Medical, 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: EWL)
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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