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FDA 510(k)

BILATERAL CONTINUOUS PASSIVE MOTION DEVICE

K-Number: K871981 · 1987-06-17

Decision Date1987-06-17
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BILATERAL CONTINUOUS PASSIVE MOTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Avec Scientific Design Corp.. It received FDA 510(k) clearance on 1987-06-17 under 510(k) number K871981. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BILATERAL CONTINUOUS PASSIVE MOTION DEVICE?

BILATERAL CONTINUOUS PASSIVE MOTION DEVICE is a medical device that received FDA 510(k) clearance on 1987-06-17. The listed applicant is Avec Scientific Design Corp.. The 510(k) number is K871981.

When did BILATERAL CONTINUOUS PASSIVE MOTION DEVICE receive FDA 510(k) clearance?

BILATERAL CONTINUOUS PASSIVE MOTION DEVICE received FDA 510(k) clearance on 1987-06-17, under 510(k) number K871981.

Who is the listed applicant for BILATERAL CONTINUOUS PASSIVE MOTION DEVICE?

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

What is the FDA product code for BILATERAL CONTINUOUS PASSIVE MOTION DEVICE?

The FDA product code for BILATERAL CONTINUOUS PASSIVE MOTION DEVICE is BXB.

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 Avec Scientific Design 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: BXB)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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