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FDA 510(k)

VENTI-SCAN II

K-Number: K871868 · 1988-04-11

ApplicantAtomic Products Corp.
Decision Date1988-04-11
Product CodeIYT
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VENTI-SCAN II is the device name listed in this FDA 510(k) record. The listed applicant is Atomic Products Corp.. It received FDA 510(k) clearance on 1988-04-11 under 510(k) number K871868. The device is classified under product code IYT. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTI-SCAN II?

VENTI-SCAN II is a medical device that received FDA 510(k) clearance on 1988-04-11. The listed applicant is Atomic Products Corp.. The 510(k) number is K871868.

When did VENTI-SCAN II receive FDA 510(k) clearance?

VENTI-SCAN II received FDA 510(k) clearance on 1988-04-11, under 510(k) number K871868.

Who is the listed applicant for VENTI-SCAN II?

The FDA 510(k) record lists Atomic Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTI-SCAN II?

The FDA product code for VENTI-SCAN II is IYT.

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Other records listing Atomic Products 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.

K915541SPECT TABLE, MODEL #056-760K913055THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900K904187ECONOMY C-ARM TABLE, MODEL # 056-005K904623RADIOGRAPHIC TRANSPORT, TRAUMA MODEL 056-230, 235K900851DIGITAL IMAGE ENHANCEMENT SYSTEMK895799RECTILINEAR SCANNER MODEL #187-270

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Related Devices (Code: IYT)

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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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