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FDA 510(k)

GASTROINTESTINAL FLEXIBLE BIOSPY FORCEPS

K-Number: K873248 · 1987-12-30

ApplicantMedical Engineering Laboratory, Inc.
Decision Date1987-12-30
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GASTROINTESTINAL FLEXIBLE BIOSPY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Engineering Laboratory, Inc.. It received FDA 510(k) clearance on 1987-12-30 under 510(k) number K873248. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GASTROINTESTINAL FLEXIBLE BIOSPY FORCEPS?

GASTROINTESTINAL FLEXIBLE BIOSPY FORCEPS is a medical device that received FDA 510(k) clearance on 1987-12-30. The listed applicant is Medical Engineering Laboratory, Inc.. The 510(k) number is K873248.

When did GASTROINTESTINAL FLEXIBLE BIOSPY FORCEPS receive FDA 510(k) clearance?

GASTROINTESTINAL FLEXIBLE BIOSPY FORCEPS received FDA 510(k) clearance on 1987-12-30, under 510(k) number K873248.

Who is the listed applicant for GASTROINTESTINAL FLEXIBLE BIOSPY FORCEPS?

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

What is the FDA product code for GASTROINTESTINAL FLEXIBLE BIOSPY FORCEPS?

The FDA product code for GASTROINTESTINAL FLEXIBLE BIOSPY FORCEPS is OCZ.

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.

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Other records listing Medical Engineering Laboratory, 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.

K973071TRI TALON RETRIEVAL FORCEPS

Related Devices (Code: OCZ)

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.

K252800KARL STORZ Endoscopic Accessories for UrologyKarl Storz SE & CO. KGK242923SimpleSnip Endoscopic Suture Cutter (SC500160); SimpleSnip Endoscopic Suture Cutter (SC500230)Envision EndoscopyK191900Single Use Grasping ForcepsZhejiang Chuangxiang Medical Technology Co., Ltd.K152802Grasping ForcepsMicro-Tech (Nanjing) Co., Ltd.K120084ENDOSCOPIC RETRIEVAL DEVICEUnited States Endoscopy Group, Inc.K103688G-PROX EZ ENDOSCOPIC GRASPERUsgi Medical

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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