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FDA 510(k)

LAPAROSCOPIC IRRIGATOR/ASPIRATOR

K-Number: K910209 · 1991-04-29

ApplicantSolos Mfg.
Decision Date1991-04-29
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC IRRIGATOR/ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Solos Mfg.. It received FDA 510(k) clearance on 1991-04-29 under 510(k) number K910209. 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 LAPAROSCOPIC IRRIGATOR/ASPIRATOR?

LAPAROSCOPIC IRRIGATOR/ASPIRATOR is a medical device that received FDA 510(k) clearance on 1991-04-29. The listed applicant is Solos Mfg.. The 510(k) number is K910209.

When did LAPAROSCOPIC IRRIGATOR/ASPIRATOR receive FDA 510(k) clearance?

LAPAROSCOPIC IRRIGATOR/ASPIRATOR received FDA 510(k) clearance on 1991-04-29, under 510(k) number K910209.

Who is the listed applicant for LAPAROSCOPIC IRRIGATOR/ASPIRATOR?

The FDA 510(k) record lists Solos Mfg. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPAROSCOPIC IRRIGATOR/ASPIRATOR?

The FDA product code for LAPAROSCOPIC IRRIGATOR/ASPIRATOR 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.

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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