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FDA 510(k)

TISSUE ISOLATION AND RETRIEVAL BAG

K-Number: K931886 · 1993-09-07

ApplicantAdvanced Surgical, Inc.
Decision Date1993-09-07
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TISSUE ISOLATION AND RETRIEVAL BAG is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Surgical, Inc.. It received FDA 510(k) clearance on 1993-09-07 under 510(k) number K931886. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TISSUE ISOLATION AND RETRIEVAL BAG?

TISSUE ISOLATION AND RETRIEVAL BAG is a medical device that received FDA 510(k) clearance on 1993-09-07. The listed applicant is Advanced Surgical, Inc.. The 510(k) number is K931886.

When did TISSUE ISOLATION AND RETRIEVAL BAG receive FDA 510(k) clearance?

TISSUE ISOLATION AND RETRIEVAL BAG received FDA 510(k) clearance on 1993-09-07, under 510(k) number K931886.

Who is the listed applicant for TISSUE ISOLATION AND RETRIEVAL BAG?

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

What is the FDA product code for TISSUE ISOLATION AND RETRIEVAL BAG?

The FDA product code for TISSUE ISOLATION AND RETRIEVAL BAG is KGX.

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Other records listing Advanced Surgical, 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.

K950126ENDOSCOPIC LIGATION DEVICE, LIGATOR HANDLE, LIGATOR CARTRIDGEK950005TROCAR CANNULA STABILIZERK945369LAPAROSCOPIC SURGICAL INSTRUMENTS FOR GENERAL USEK933497LAPAROSCOPIC COVERED SURGICAL RETRACTORK941500TISSUE ISOLATION AND RETRIEVAL BAGK931850VERRSS PNEUMO NEEDLE

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Related Devices (Code: KGX)

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.

K001240SERAGARD INJECTION PATCHPlatinum Services, Inc.K983368CARE BAND ANTIBACTERIAL BANDAGESAso Corp.K972914SYVEK PATCHMarine Polymer Technologies, Inc.K943314ADHESIVE BANDAGES WITH OTC DRUGJohnson & Johnson Consumer Products, Inc.K952606TARGETT PATCHCutting Edge Technologies, Inc.K954007PARALLELJohnson & Johnson Consumer Products, Inc.

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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