DANIELL DBL PUNCTURE LASER LAPAROSCOPY
K-Number: K842498 · 1984-09-25
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Device Summary
Frequently Asked Questions
What is the DANIELL DBL PUNCTURE LASER LAPAROSCOPY?
DANIELL DBL PUNCTURE LASER LAPAROSCOPY is a medical device that received FDA 510(k) clearance on 1984-09-25. The listed applicant is Laser Spectrum, Inc.. The 510(k) number is K842498.
When did DANIELL DBL PUNCTURE LASER LAPAROSCOPY receive FDA 510(k) clearance?
DANIELL DBL PUNCTURE LASER LAPAROSCOPY received FDA 510(k) clearance on 1984-09-25, under 510(k) number K842498.
Who is the listed applicant for DANIELL DBL PUNCTURE LASER LAPAROSCOPY?
The FDA 510(k) record lists Laser Spectrum, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DANIELL DBL PUNCTURE LASER LAPAROSCOPY?
The FDA product code for DANIELL DBL PUNCTURE LASER LAPAROSCOPY 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 Laser Spectrum, 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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