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FDA 510(k)

MONOJECT SCALE MAGNIFIER

K-Number: K781459 · 1978-10-24

ApplicantSherwood Medical Industries
Decision Date1978-10-24
Product CodeHJY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MONOJECT SCALE MAGNIFIER 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 1978-10-24 under 510(k) number K781459. The device is classified under product code HJY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOJECT SCALE MAGNIFIER?

MONOJECT SCALE MAGNIFIER is a medical device that received FDA 510(k) clearance on 1978-10-24. The listed applicant is Sherwood Medical Industries. The 510(k) number is K781459.

When did MONOJECT SCALE MAGNIFIER receive FDA 510(k) clearance?

MONOJECT SCALE MAGNIFIER received FDA 510(k) clearance on 1978-10-24, under 510(k) number K781459.

Who is the listed applicant for MONOJECT SCALE MAGNIFIER?

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 MONOJECT SCALE MAGNIFIER?

The FDA product code for MONOJECT SCALE MAGNIFIER is HJY.

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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 SERUMK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPE

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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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