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FDA 510(k)

FLUOROSCOPE BAND BAG

K-Number: K861785 · 1986-06-13

Decision Date1986-06-13
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FLUOROSCOPE BAND BAG is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Plast Intl., Inc.. It received FDA 510(k) clearance on 1986-06-13 under 510(k) number K861785. 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 FLUOROSCOPE BAND BAG?

FLUOROSCOPE BAND BAG is a medical device that received FDA 510(k) clearance on 1986-06-13. The listed applicant is Medi-Plast Intl., Inc.. The 510(k) number is K861785.

When did FLUOROSCOPE BAND BAG receive FDA 510(k) clearance?

FLUOROSCOPE BAND BAG received FDA 510(k) clearance on 1986-06-13, under 510(k) number K861785.

Who is the listed applicant for FLUOROSCOPE BAND BAG?

The FDA 510(k) record lists Medi-Plast Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLUOROSCOPE BAND BAG?

The FDA product code for FLUOROSCOPE BAND BAG 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.

Other records listing Medi-Plast Intl., Inc. 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.

View all 12 devices →

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.

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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