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FDA 510(k)

LAPOROSCOPIC SCISSORS

K-Number: K942431 · 1995-10-11

ApplicantEnterprise Medical Corp.
Decision Date1995-10-11
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LAPOROSCOPIC SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Enterprise Medical Corp.. It received FDA 510(k) clearance on 1995-10-11 under 510(k) number K942431. 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 LAPOROSCOPIC SCISSORS?

LAPOROSCOPIC SCISSORS is a medical device that received FDA 510(k) clearance on 1995-10-11. The listed applicant is Enterprise Medical Corp.. The 510(k) number is K942431.

When did LAPOROSCOPIC SCISSORS receive FDA 510(k) clearance?

LAPOROSCOPIC SCISSORS received FDA 510(k) clearance on 1995-10-11, under 510(k) number K942431.

Who is the listed applicant for LAPOROSCOPIC SCISSORS?

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

What is the FDA product code for LAPOROSCOPIC SCISSORS?

The FDA product code for LAPOROSCOPIC SCISSORS is HET.

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Other records listing Enterprise Medical Corp. 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.

K943583KERRISON RONGEURSK941816EMC FLEXIBLE BIOPSY FORCEPS

Related Devices (Code: HET)

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Official Source

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