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FDA 510(k)

STERILE LAPAROTOMY SPONGES

K-Number: K934971 · 1994-02-07

Decision Date1994-02-07
Product CodeGDY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE LAPAROTOMY SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Medsurg Industries, Inc.. It received FDA 510(k) clearance on 1994-02-07 under 510(k) number K934971. The device is classified under product code GDY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE LAPAROTOMY SPONGES?

STERILE LAPAROTOMY SPONGES is a medical device that received FDA 510(k) clearance on 1994-02-07. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K934971.

When did STERILE LAPAROTOMY SPONGES receive FDA 510(k) clearance?

STERILE LAPAROTOMY SPONGES received FDA 510(k) clearance on 1994-02-07, under 510(k) number K934971.

Who is the listed applicant for STERILE LAPAROTOMY SPONGES?

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

What is the FDA product code for STERILE LAPAROTOMY SPONGES?

The FDA product code for STERILE LAPAROTOMY SPONGES is GDY.

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 Medsurg Industries, 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 41 devices →

Related Devices (Code: GDY)

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

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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