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FDA 510(k)

LANCER ICE CUBE

K-Number: K782077 · 1979-04-03

ApplicantSherwood Medical Industries
Decision Date1979-04-03
Product CodeJRM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LANCER ICE CUBE 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 1979-04-03 under 510(k) number K782077. The device is classified under product code JRM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANCER ICE CUBE?

LANCER ICE CUBE is a medical device that received FDA 510(k) clearance on 1979-04-03. The listed applicant is Sherwood Medical Industries. The 510(k) number is K782077.

When did LANCER ICE CUBE receive FDA 510(k) clearance?

LANCER ICE CUBE received FDA 510(k) clearance on 1979-04-03, under 510(k) number K782077.

Who is the listed applicant for LANCER ICE CUBE?

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 ICE CUBE?

The FDA product code for LANCER ICE CUBE is JRM.

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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 SERUMK790523ARGYLE ESOPHAGEAL STETHOSCOPEK790196MONOJECT ARTERIAL BLOOD SAMPLING DEVICE

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Related Devices (Code: JRM)

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.

K921569ORS-200Mnlase, Inc.K921570ORS-300Mnlase, Inc.K921568ORS-100Mnlase, Inc.K915427ORS-1000Mnlase, Inc.K913777SELF-CONTAINED SURGICAL SLUSH FREEZERTaylor Corp.K894006SANISERV SURGICAL SLUSH SYSTEMSaniserv, 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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