Miniaturized Biopsy,Scope A.K.A: Biopsy Needle with Endoscopic Viewing Capability

FDA 510(k) K983538 · Solos Endoscopy, Inc.

Substantially Equivalent

510(k) numberK983538

Submission

Device name
Miniaturized Biopsy,Scope A.K.A: Biopsy Needle with Endoscopic Viewing Capability
Applicant
Solos Endoscopy, Inc.
Braintree, MA, US
Received
October 9, 1998
Decision date
November 6, 1998
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GCJ – Laparoscope, General & Plastic Surgery
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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Questions and answers

When was Miniaturized Biopsy,Scope A.K.A: Biopsy Needle with Endoscopic Viewing Capability cleared by the FDA?

Miniaturized Biopsy,Scope A.K.A: Biopsy Needle with Endoscopic Viewing Capability (K983538) received a 510(k) decision of Substantially Equivalent on November 6, 1998, 28 days after the submission was received.

What is the product code of K983538?

The FDA product code is GCJ – Laparoscope, General & Plastic Surgery, a Class II (moderate risk) device regulated under 21 CFR 876.1500.