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FDA 510(k)

LAPSTICK LAPAROSCOPIC SPONGE STICK/ BLUNT DISSEC.

K-Number: K922987 · 1993-04-23

Decision Date1993-04-23
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPSTICK LAPAROSCOPIC SPONGE STICK/ BLUNT DISSEC. is the device name listed in this FDA 510(k) record. The listed applicant is Biosearch Medical Products, Inc.. It received FDA 510(k) clearance on 1993-04-23 under 510(k) number K922987. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPSTICK LAPAROSCOPIC SPONGE STICK/ BLUNT DISSEC.?

LAPSTICK LAPAROSCOPIC SPONGE STICK/ BLUNT DISSEC. is a medical device that received FDA 510(k) clearance on 1993-04-23. The listed applicant is Biosearch Medical Products, Inc.. The 510(k) number is K922987.

When did LAPSTICK LAPAROSCOPIC SPONGE STICK/ BLUNT DISSEC. receive FDA 510(k) clearance?

LAPSTICK LAPAROSCOPIC SPONGE STICK/ BLUNT DISSEC. received FDA 510(k) clearance on 1993-04-23, under 510(k) number K922987.

Who is the listed applicant for LAPSTICK LAPAROSCOPIC SPONGE STICK/ BLUNT DISSEC.?

The FDA 510(k) record lists Biosearch Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPSTICK LAPAROSCOPIC SPONGE STICK/ BLUNT DISSEC.?

The FDA product code for LAPSTICK LAPAROSCOPIC SPONGE STICK/ BLUNT DISSEC. is GCJ.

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.

Other records listing Biosearch Medical Products, Inc. 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.

View all 70 devices →

Related Devices (Code: GCJ)

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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