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FDA 510(k)

CHART PROJECTOR

K-Number: K821081 · 1982-06-14

ApplicantMedical Equipment Designs, Inc.
Decision Date1982-06-14
Product CodeHOJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CHART PROJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Equipment Designs, Inc.. It received FDA 510(k) clearance on 1982-06-14 under 510(k) number K821081. The device is classified under product code HOJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHART PROJECTOR?

CHART PROJECTOR is a medical device that received FDA 510(k) clearance on 1982-06-14. The listed applicant is Medical Equipment Designs, Inc.. The 510(k) number is K821081.

When did CHART PROJECTOR receive FDA 510(k) clearance?

CHART PROJECTOR received FDA 510(k) clearance on 1982-06-14, under 510(k) number K821081.

Who is the listed applicant for CHART PROJECTOR?

The FDA 510(k) record lists Medical Equipment Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHART PROJECTOR?

The FDA product code for CHART PROJECTOR is HOJ.

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Other records listing Medical Equipment Designs, Inc. 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.

K911308CARDIOTRACE-I TRANSTELEPHONIC ECG RECEIV CONSOLEK894152MEDITHERMK895375MULTISPIROK851277MICROSPIRO-SDSK840929FRC 85 SERIES SPIROMETERK840908CHESTAC-25F SPIROMETER

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Related Devices (Code: HOJ)

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.

K873919TANGENT SCREENRichmond Products, Inc.K844657SPECTABLE FRAME MAGNIFYING BRILLETTEPro Design Intl. AS

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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