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FDA 510(k)

PORTACAMERA 11-B

K-Number: K761159 · 1976-12-06

ApplicantGeneral Electric Co.
Decision Date1976-12-06
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PORTACAMERA 11-B is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1976-12-06 under 510(k) number K761159. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTACAMERA 11-B?

PORTACAMERA 11-B is a medical device that received FDA 510(k) clearance on 1976-12-06. The listed applicant is General Electric Co.. The 510(k) number is K761159.

When did PORTACAMERA 11-B receive FDA 510(k) clearance?

PORTACAMERA 11-B received FDA 510(k) clearance on 1976-12-06, under 510(k) number K761159.

Who is the listed applicant for PORTACAMERA 11-B?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTACAMERA 11-B?

The FDA product code for PORTACAMERA 11-B is IYX.

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Related Devices (Code: IYX)

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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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