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FDA 510(k)

LAPAROSCOPY CONSOLE MODEL VIII

K-Number: K772242 · 1977-12-20

ApplicantKli
Decision Date1977-12-20
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPY CONSOLE MODEL VIII is the device name listed in this FDA 510(k) record. The listed applicant is Kli. It received FDA 510(k) clearance on 1977-12-20 under 510(k) number K772242. 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 LAPAROSCOPY CONSOLE MODEL VIII?

LAPAROSCOPY CONSOLE MODEL VIII is a medical device that received FDA 510(k) clearance on 1977-12-20. The listed applicant is Kli. The 510(k) number is K772242.

When did LAPAROSCOPY CONSOLE MODEL VIII receive FDA 510(k) clearance?

LAPAROSCOPY CONSOLE MODEL VIII received FDA 510(k) clearance on 1977-12-20, under 510(k) number K772242.

Who is the listed applicant for LAPAROSCOPY CONSOLE MODEL VIII?

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

What is the FDA product code for LAPAROSCOPY CONSOLE MODEL VIII?

The FDA product code for LAPAROSCOPY CONSOLE MODEL VIII is HET.

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Other records listing Kli 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.

K800822CO2 CYSTOSCOPY/URETHROSCOPY CONSOLEK800913GYNECOLOGICAL CYSTO/URETHROSCOPEK781913INSUFFALATOR LAPARAOSCOPICK781109FORCEPS, ELECTROSURGICALK781089ONE INCISION BI-POLAR ELECTRO. FORCEPSK780955SCISSORS, HOOK, ELECTROSURGICAL

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Related Devices (Code: HET)

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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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