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FDA 510(k)

DANIELL DBL PUNCTURE LASER LAPAROSCOPY

K-Number: K842498 · 1984-09-25

Decision Date1984-09-25
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DANIELL DBL PUNCTURE LASER LAPAROSCOPY is the device name listed in this FDA 510(k) record. The listed applicant is Laser Spectrum, Inc.. It received FDA 510(k) clearance on 1984-09-25 under 510(k) number K842498. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

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

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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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