FDA 510(k)

STRYKER MODEL 977 BIRTHING BED

K-Number: K870745 · 1987-02-27

Decision Date1987-02-27

Product CodeKNC

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

STRYKER MODEL 977 BIRTHING BED is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1987-02-27 under 510(k) number K870745. The device is classified under product code KNC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER MODEL 977 BIRTHING BED?

STRYKER MODEL 977 BIRTHING BED is a medical device that received FDA 510(k) clearance on 1987-02-27. The listed applicant is Stryker Corp.. The 510(k) number is K870745.

When did STRYKER MODEL 977 BIRTHING BED receive FDA 510(k) clearance?

STRYKER MODEL 977 BIRTHING BED received FDA 510(k) clearance on 1987-02-27, under 510(k) number K870745.

Who is the listed applicant for STRYKER MODEL 977 BIRTHING BED?

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

What is the FDA product code for STRYKER MODEL 977 BIRTHING BED?

The FDA product code for STRYKER MODEL 977 BIRTHING BED is KNC.

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Other records listing Stryker Corp. as applicant

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Related Devices (Code: KNC)

K001261L720 EXAMINATION CHAIRLuneau Gynecologie SA K932035NON-LINTING DELIVERY BLANKETAmsco Sterile Recoveries, Inc.K924420MEDICAL DISPOSABLE BEDDINGHill-Rom, Inc.K914544BD6000 THE OPTIMA & BD5000 BIRTHING BEDLic Care, Inc.K915779AFFINITY BED MODEL 3600 SERIESHill-Rom, Inc.K903973GARDOSI BIRTHING CUSHIONGraphic Controls Corp.

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.