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FDA 510(k)

BTP(TM) CENTRALINE(TM) SUIT

K-Number: K914615 · 1992-05-05

ApplicantBtp Industries, Inc.
Decision Date1992-05-05
Product CodeFXO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BTP(TM) CENTRALINE(TM) SUIT is the device name listed in this FDA 510(k) record. The listed applicant is Btp Industries, Inc.. It received FDA 510(k) clearance on 1992-05-05 under 510(k) number K914615. The device is classified under product code FXO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BTP(TM) CENTRALINE(TM) SUIT?

BTP(TM) CENTRALINE(TM) SUIT is a medical device that received FDA 510(k) clearance on 1992-05-05. The listed applicant is Btp Industries, Inc.. The 510(k) number is K914615.

When did BTP(TM) CENTRALINE(TM) SUIT receive FDA 510(k) clearance?

BTP(TM) CENTRALINE(TM) SUIT received FDA 510(k) clearance on 1992-05-05, under 510(k) number K914615.

Who is the listed applicant for BTP(TM) CENTRALINE(TM) SUIT?

The FDA 510(k) record lists Btp Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BTP(TM) CENTRALINE(TM) SUIT?

The FDA product code for BTP(TM) CENTRALINE(TM) SUIT is FXO.

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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Related Devices (Code: FXO)

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.

K891212APRONS, SCRUBS SLACKS & TOPS, PATIENT DRAPEPro-Safe Professional Linens, Inc.K882282SUIT, SURGICALA Plus International, Inc.K865022SURGICAL GARMENTSUlti-Med Intl., Inc.K831207SPUNGUARD SCRUB SUITKimberly-Clark Corp.K822483MULTIPLE SCRUB SUITSurgilite Intl., Inc.

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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