BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO
K-Number: K790877 · 1979-05-23
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Device Summary
Frequently Asked Questions
What is the BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO?
BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO is a medical device that received FDA 510(k) clearance on 1979-05-23. The listed applicant is Stackhouse Assoc.. The 510(k) number is K790877.
When did BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO receive FDA 510(k) clearance?
BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO received FDA 510(k) clearance on 1979-05-23, under 510(k) number K790877.
Who is the listed applicant for BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO?
The FDA 510(k) record lists Stackhouse Assoc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO?
The FDA product code for BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO is JDY.
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 Stackhouse Assoc. 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: JDY)
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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