CINE CAMERA CONTROL MODEL PK2037
K-Number: K896615 · 1990-01-04
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Device Summary
Frequently Asked Questions
What is the CINE CAMERA CONTROL MODEL PK2037?
CINE CAMERA CONTROL MODEL PK2037 is a medical device that received FDA 510(k) clearance on 1990-01-04. The listed applicant is Perkins Mfg. Co.. The 510(k) number is K896615.
When did CINE CAMERA CONTROL MODEL PK2037 receive FDA 510(k) clearance?
CINE CAMERA CONTROL MODEL PK2037 received FDA 510(k) clearance on 1990-01-04, under 510(k) number K896615.
Who is the listed applicant for CINE CAMERA CONTROL MODEL PK2037?
The FDA 510(k) record lists Perkins Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CINE CAMERA CONTROL MODEL PK2037?
The FDA product code for CINE CAMERA CONTROL MODEL PK2037 is IZJ.
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 Perkins Mfg. Co. 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: IZJ)
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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