POLAROID LAND CAMERA FOR ENDOSCOPY
K-Number: K792512 · 1979-12-20
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Device Summary
Frequently Asked Questions
What is the POLAROID LAND CAMERA FOR ENDOSCOPY?
POLAROID LAND CAMERA FOR ENDOSCOPY is a medical device that received FDA 510(k) clearance on 1979-12-20. The listed applicant is Polaroid Corp.. The 510(k) number is K792512.
When did POLAROID LAND CAMERA FOR ENDOSCOPY receive FDA 510(k) clearance?
POLAROID LAND CAMERA FOR ENDOSCOPY received FDA 510(k) clearance on 1979-12-20, under 510(k) number K792512.
Who is the listed applicant for POLAROID LAND CAMERA FOR ENDOSCOPY?
The FDA 510(k) record lists Polaroid Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POLAROID LAND CAMERA FOR ENDOSCOPY?
The FDA product code for POLAROID LAND CAMERA FOR ENDOSCOPY is FEM.
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 Polaroid Corp. 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.
Related Devices (Code: FEM)
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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