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FDA 510(k)

BODAI M.D.D. ADAPTOR(TM)

K-Number: K881849 · 1988-07-01

ApplicantB&B Medical Technologies, Inc.
Decision Date1988-07-01
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BODAI M.D.D. ADAPTOR(TM) is the device name listed in this FDA 510(k) record. The listed applicant is B&B Medical Technologies, Inc.. It received FDA 510(k) clearance on 1988-07-01 under 510(k) number K881849. The device is classified under product code BZA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BODAI M.D.D. ADAPTOR(TM)?

BODAI M.D.D. ADAPTOR(TM) is a medical device that received FDA 510(k) clearance on 1988-07-01. The listed applicant is B&B Medical Technologies, Inc.. The 510(k) number is K881849.

When did BODAI M.D.D. ADAPTOR(TM) receive FDA 510(k) clearance?

BODAI M.D.D. ADAPTOR(TM) received FDA 510(k) clearance on 1988-07-01, under 510(k) number K881849.

Who is the listed applicant for BODAI M.D.D. ADAPTOR(TM)?

The FDA 510(k) record lists B&B Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BODAI M.D.D. ADAPTOR(TM)?

The FDA product code for BODAI M.D.D. ADAPTOR(TM) is BZA.

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 B&B Medical Technologies, 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.

K030396OMNI~NEB; OMNI~MAXK980407HOPE NEBULIZERK960663UNIVERSAL BITE BLOCKK945816QUICK-LOCKK944324SURE-LOCK VENTILATOR TUBING HOLDERK935171STABILTRACH

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Related Devices (Code: BZA)

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.

K083702TRACH-ASSISTMergenet MedicalK954383SURELOC CIRCUIT CONNECTORPolamedco, Inc.K954197DISPOSABLE FLEX TUBEEngstrom MedicalK953786UNICOR, INC. CONNECTORS & AIRWAY EXTENSIONSUnicor, Inc.K952824NEO-LINK, DISPOSABLE NEONATAL AIR WAY CONNECTORIntertex Medical, Inc.K951345DISPOSABLE AIRWAY CONNECTORS FOR GAS SAMPLINGCatheter Research, Inc.

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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