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FDA 510(k)

LANCER L-INA BUFFER, POLYMER, WASH SOLU

K-Number: K792014 · 1979-11-13

ApplicantSherwood Medical Industries
Decision Date1979-11-13
Product CodeJZW
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LANCER L-INA BUFFER, POLYMER, WASH SOLU 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 1979-11-13 under 510(k) number K792014. The device is classified under product code JZW. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANCER L-INA BUFFER, POLYMER, WASH SOLU?

LANCER L-INA BUFFER, POLYMER, WASH SOLU is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Sherwood Medical Industries. The 510(k) number is K792014.

When did LANCER L-INA BUFFER, POLYMER, WASH SOLU receive FDA 510(k) clearance?

LANCER L-INA BUFFER, POLYMER, WASH SOLU received FDA 510(k) clearance on 1979-11-13, under 510(k) number K792014.

Who is the listed applicant for LANCER L-INA BUFFER, POLYMER, WASH SOLU?

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 L-INA BUFFER, POLYMER, WASH SOLU?

The FDA product code for LANCER L-INA BUFFER, POLYMER, WASH SOLU is JZW.

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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 KITK792013LANCER L-INA HUMAN REFERENCE SERUMK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPEK790196MONOJECT ARTERIAL BLOOD SAMPLING DEVICE

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Related Devices (Code: JZW)

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.

K001647BN PROSPEC SYSTEMDade Behring, Inc.K761234BEHRING LASER NEPHELOMETERBehring Diagnostics, Inc.K892223BEHRING NEPHELOMETER 100Behring Diagnostics, Inc.K873407RRT SYSTEM LASER REFLECTOMETER ANALYZERIncstar Corp.K873401TURBOXUnipath , Ltd.K801949BCM-302 COLLIMATING CONE & COMPENSATINB C Medical , Ltd.

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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