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FDA 510(k)

LANCER AUTOANALYZER MANIFOLD PUMP TUB

K-Number: K760622 · 1976-11-24

ApplicantSherwood Medical Industries
Decision Date1976-11-24
Product CodeJJC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LANCER AUTOANALYZER MANIFOLD PUMP TUB is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1976-11-24 under 510(k) number K760622. 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 AUTOANALYZER MANIFOLD PUMP TUB?

LANCER AUTOANALYZER MANIFOLD PUMP TUB is a medical device that received FDA 510(k) clearance on 1976-11-24. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760622.

When did LANCER AUTOANALYZER MANIFOLD PUMP TUB receive FDA 510(k) clearance?

LANCER AUTOANALYZER MANIFOLD PUMP TUB received FDA 510(k) clearance on 1976-11-24, under 510(k) number K760622.

Who is the listed applicant for LANCER AUTOANALYZER MANIFOLD PUMP TUB?

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

What is the FDA product code for LANCER AUTOANALYZER MANIFOLD PUMP TUB?

The FDA product code for LANCER AUTOANALYZER MANIFOLD PUMP TUB is JJC.

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Other records listing Sherwood Medical Industries 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.

K801070SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLESK801071LANCER GLUCOSE RATE REAGENT KITK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK792013LANCER L-INA HUMAN REFERENCE SERUMK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPE

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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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