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FDA 510(k)

LANCER ANALYZER CUPS

K-Number: K833157 · 1983-12-08

ApplicantSherwood Medical Co.
Decision Date1983-12-08
Product CodeJJC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LANCER ANALYZER CUPS is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1983-12-08 under 510(k) number K833157. The device is classified under product code JJC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANCER ANALYZER CUPS?

LANCER ANALYZER CUPS is a medical device that received FDA 510(k) clearance on 1983-12-08. The listed applicant is Sherwood Medical Co.. The 510(k) number is K833157.

When did LANCER ANALYZER CUPS receive FDA 510(k) clearance?

LANCER ANALYZER CUPS received FDA 510(k) clearance on 1983-12-08, under 510(k) number K833157.

Who is the listed applicant for LANCER ANALYZER CUPS?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LANCER ANALYZER CUPS?

The FDA product code for LANCER ANALYZER CUPS is JJC.

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Other records listing Sherwood Medical Co. 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.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

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Related Devices (Code: JJC)

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.

K945915AVL OMNI ANALYZERAvl Scientific Corp.K945584NOVA 16 ANALYZERNova Biomedical Corp.K943376OPERA SYSTEMMiles, Inc.K901410TECHNICON RA-2000(TM) SYSTEMTechnicon Instruments Corp.K901141PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZXBaxter Healthcare CorpK890332RFA/2 RAPID FLOW ANALYZER W/COMPUTERAlpkem Corp.

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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