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FDA 510(k)

VIDEO ADAPTER FOR GRAPHIC RECORDERS

K-Number: K772012 · 1977-11-07

Decision Date1977-11-07
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIDEO ADAPTER FOR GRAPHIC RECORDERS is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1977-11-07 under 510(k) number K772012. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDEO ADAPTER FOR GRAPHIC RECORDERS?

VIDEO ADAPTER FOR GRAPHIC RECORDERS is a medical device that received FDA 510(k) clearance on 1977-11-07. The listed applicant is Honeywell, Inc.. The 510(k) number is K772012.

When did VIDEO ADAPTER FOR GRAPHIC RECORDERS receive FDA 510(k) clearance?

VIDEO ADAPTER FOR GRAPHIC RECORDERS received FDA 510(k) clearance on 1977-11-07, under 510(k) number K772012.

Who is the listed applicant for VIDEO ADAPTER FOR GRAPHIC RECORDERS?

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

What is the FDA product code for VIDEO ADAPTER FOR GRAPHIC RECORDERS?

The FDA product code for VIDEO ADAPTER FOR GRAPHIC RECORDERS is IYO.

Related Clinical Trials

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.

Other records listing Honeywell, 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.

View all 69 devices →

Related Devices (Code: IYO)

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.

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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