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FDA 510(k)

LANCER MSA BUN DIAG. KIT

K-Number: K821562 · 1982-06-11

ApplicantSherwood Medical Co.
Decision Date1982-06-11
Product CodeCDQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LANCER MSA BUN DIAG. KIT 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 1982-06-11 under 510(k) number K821562. The device is classified under product code CDQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANCER MSA BUN DIAG. KIT?

LANCER MSA BUN DIAG. KIT is a medical device that received FDA 510(k) clearance on 1982-06-11. The listed applicant is Sherwood Medical Co.. The 510(k) number is K821562.

When did LANCER MSA BUN DIAG. KIT receive FDA 510(k) clearance?

LANCER MSA BUN DIAG. KIT received FDA 510(k) clearance on 1982-06-11, under 510(k) number K821562.

Who is the listed applicant for LANCER MSA BUN DIAG. KIT?

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 MSA BUN DIAG. KIT?

The FDA product code for LANCER MSA BUN DIAG. KIT is CDQ.

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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: CDQ)

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.

K203771Urea Nitrogen2Abbott Ireland Diagnostics DivisionK110675EASYRA UREA NITROGEN AND CREATININE REAGENTSMedica Corp.K073295UREA/BUN, SCAL, NORTROL, ABTROLThermofisher Scientific OYK070146ABX PENTRA GLUCOSE HK CP, UREA CP, URIC ACID CPHoriba AbxK060120TECO CX3 REAGENT SET FOR SYNCHRON CX SYSTEMTeco DiagnosticsK041051RAICHEM BUN RATE REAGENT (LIQUID)Hemagen Diagnostics, 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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