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FDA 510(k)

STRYKER OPERATING LAPAROSCOPE

K-Number: K943100 · 1995-08-10

ApplicantStryker Endoscopy
Decision Date1995-08-10
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

STRYKER OPERATING LAPAROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 1995-08-10 under 510(k) number K943100. 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 STRYKER OPERATING LAPAROSCOPE?

STRYKER OPERATING LAPAROSCOPE is a medical device that received FDA 510(k) clearance on 1995-08-10. The listed applicant is Stryker Endoscopy. The 510(k) number is K943100.

When did STRYKER OPERATING LAPAROSCOPE receive FDA 510(k) clearance?

STRYKER OPERATING LAPAROSCOPE received FDA 510(k) clearance on 1995-08-10, under 510(k) number K943100.

Who is the listed applicant for STRYKER OPERATING LAPAROSCOPE?

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

What is the FDA product code for STRYKER OPERATING LAPAROSCOPE?

The FDA product code for STRYKER OPERATING LAPAROSCOPE 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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