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FDA 510(k)

PLASTIC SHOWER GUARD

K-Number: K791646 · 1979-10-01

ApplicantB & F Medical Products, Inc.
Decision Date1979-10-01
Product CodeKIA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PLASTIC SHOWER GUARD is the device name listed in this FDA 510(k) record. The listed applicant is B & F Medical Products, Inc.. It received FDA 510(k) clearance on 1979-10-01 under 510(k) number K791646. The device is classified under product code KIA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLASTIC SHOWER GUARD?

PLASTIC SHOWER GUARD is a medical device that received FDA 510(k) clearance on 1979-10-01. The listed applicant is B & F Medical Products, Inc.. The 510(k) number is K791646.

When did PLASTIC SHOWER GUARD receive FDA 510(k) clearance?

PLASTIC SHOWER GUARD received FDA 510(k) clearance on 1979-10-01, under 510(k) number K791646.

Who is the listed applicant for PLASTIC SHOWER GUARD?

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

What is the FDA product code for PLASTIC SHOWER GUARD?

The FDA product code for PLASTIC SHOWER GUARD is KIA.

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Other records listing B & F Medical Products, 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.

K942645B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REGK920573CANNULA NASAL OXYGENK913501TRACHEOSTOMY MASKK861325MAXI-USE O2 DEVICEK861054DISPOSABLE RESCUE BREATHING DEVICEK853004PORTABLE OXYGEN UNIT

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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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