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FDA 510(k)

VIDEO ANNOTATOR MODEL PK2310

K-Number: K910384 · 1991-04-16

ApplicantPerkins Mfg. Co.
Decision Date1991-04-16
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIDEO ANNOTATOR MODEL PK2310 is the device name listed in this FDA 510(k) record. The listed applicant is Perkins Mfg. Co.. It received FDA 510(k) clearance on 1991-04-16 under 510(k) number K910384. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDEO ANNOTATOR MODEL PK2310?

VIDEO ANNOTATOR MODEL PK2310 is a medical device that received FDA 510(k) clearance on 1991-04-16. The listed applicant is Perkins Mfg. Co.. The 510(k) number is K910384.

When did VIDEO ANNOTATOR MODEL PK2310 receive FDA 510(k) clearance?

VIDEO ANNOTATOR MODEL PK2310 received FDA 510(k) clearance on 1991-04-16, under 510(k) number K910384.

Who is the listed applicant for VIDEO ANNOTATOR MODEL PK2310?

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 VIDEO ANNOTATOR MODEL PK2310?

The FDA product code for VIDEO ANNOTATOR MODEL PK2310 is JAA.

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.

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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.

K972136TV MONITOR (P12/17)K954222VIDEO ENHANCEMENT UNITK926348SC1000 SCAN CONVERTERK920550DISPLAY PROCESSOR - MODEL IDP5100K915232GRUNDIG ELECTRONICS VARIOUS MODELSK904986PROGRAMMABLE VIDEO CONTROLLER MODEL PK2060

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Related Devices (Code: JAA)

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.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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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