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FDA 510(k)

LAPAROSCOPE, FIBER LIGHT, PALMER-JACOBS

K-Number: K770378 · 1977-03-09

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1977-03-09
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPE, FIBER LIGHT, PALMER-JACOBS is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1977-03-09 under 510(k) number K770378. 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 LAPAROSCOPE, FIBER LIGHT, PALMER-JACOBS?

LAPAROSCOPE, FIBER LIGHT, PALMER-JACOBS is a medical device that received FDA 510(k) clearance on 1977-03-09. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K770378.

When did LAPAROSCOPE, FIBER LIGHT, PALMER-JACOBS receive FDA 510(k) clearance?

LAPAROSCOPE, FIBER LIGHT, PALMER-JACOBS received FDA 510(k) clearance on 1977-03-09, under 510(k) number K770378.

Who is the listed applicant for LAPAROSCOPE, FIBER LIGHT, PALMER-JACOBS?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPAROSCOPE, FIBER LIGHT, PALMER-JACOBS?

The FDA product code for LAPAROSCOPE, FIBER LIGHT, PALMER-JACOBS is 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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