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FDA 510(k)

LANCER PLASTIC TRANSFER PIPETTE

K-Number: K760621 · 1976-10-05

ApplicantSherwood Medical Industries
Decision Date1976-10-05
Product CodeJRC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LANCER PLASTIC TRANSFER PIPETTE 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 1976-10-05 under 510(k) number K760621. The device is classified under product code JRC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANCER PLASTIC TRANSFER PIPETTE?

LANCER PLASTIC TRANSFER PIPETTE is a medical device that received FDA 510(k) clearance on 1976-10-05. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760621.

When did LANCER PLASTIC TRANSFER PIPETTE receive FDA 510(k) clearance?

LANCER PLASTIC TRANSFER PIPETTE received FDA 510(k) clearance on 1976-10-05, under 510(k) number K760621.

Who is the listed applicant for LANCER PLASTIC TRANSFER PIPETTE?

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 PLASTIC TRANSFER PIPETTE?

The FDA product code for LANCER PLASTIC TRANSFER PIPETTE is JRC.

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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: JRC)

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.

K840186SMI DIGITRONScientific Manufacturing IndustriesK834100PRE-CALIBRATED PIPETTESVitexK822078DADE DISP. DISPENSING-SPREADING PIPETSAmerican DadeK792696MICROPITETTEMeridian Diagnostics, Inc.K770594LABORATORY EXPENDABLE PRODUCTSAbco Dealers, 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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