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FDA 510(k)

MCNEALY-GLASSMAN VISCERA RETAINER #3202/3204/3206

K-Number: K870809 · 1987-03-19

ApplicantAdept-Med Intl., Inc.
Decision Date1987-03-19
Product CodeGCZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MCNEALY-GLASSMAN VISCERA RETAINER #3202/3204/3206 is the device name listed in this FDA 510(k) record. The listed applicant is Adept-Med Intl., Inc.. It received FDA 510(k) clearance on 1987-03-19 under 510(k) number K870809. The device is classified under product code GCZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MCNEALY-GLASSMAN VISCERA RETAINER #3202/3204/3206?

MCNEALY-GLASSMAN VISCERA RETAINER #3202/3204/3206 is a medical device that received FDA 510(k) clearance on 1987-03-19. The listed applicant is Adept-Med Intl., Inc.. The 510(k) number is K870809.

When did MCNEALY-GLASSMAN VISCERA RETAINER #3202/3204/3206 receive FDA 510(k) clearance?

MCNEALY-GLASSMAN VISCERA RETAINER #3202/3204/3206 received FDA 510(k) clearance on 1987-03-19, under 510(k) number K870809.

Who is the listed applicant for MCNEALY-GLASSMAN VISCERA RETAINER #3202/3204/3206?

The FDA 510(k) record lists Adept-Med Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MCNEALY-GLASSMAN VISCERA RETAINER #3202/3204/3206?

The FDA product code for MCNEALY-GLASSMAN VISCERA RETAINER #3202/3204/3206 is GCZ.

Related Clinical Trials

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Other records listing Adept-Med Intl., 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.

K935636GRAVESPECK893871GOOTT BALFOUR BLADEK893869GOOTT MULTIPURPOSE FLEXIBLE RETRACTOR (STERILE)K893870ADAMS BREAST IMPLANT PROTECTORK802806VISECERA RETAINER

Related Devices (Code: GCZ)

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.

K904536JAIN GRAFT ASSISTJain Surgical Equipment, Inc.K893870ADAMS BREAST IMPLANT PROTECTORAdept-Med Intl., Inc.K802806VISECERA RETAINERAdept-Med Intl., Inc.K801610CHILDREN'S HOSPITAL PEDIATRIC RETRACTOREdward Weck, 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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